NM_000128.4(F11):c.809A>T (p.Lys270Ile)
|
rs121965070
|
0.00055
|
NM_000128.4(F11):c.683G>A (p.Arg228Gln)
|
rs281875246
|
0.00006
|
NM_000128.4(F11):c.943G>A (p.Glu315Lys)
|
rs281875257
|
0.00006
|
NM_000128.4(F11):c.127G>A (p.Ala43Thr)
|
rs281875264
|
0.00004
|
NM_000128.4(F11):c.723C>G (p.Phe241Leu)
|
rs281875265
|
0.00004
|
NM_000128.4(F11):c.1724C>T (p.Ser575Leu)
|
rs281875250
|
0.00003
|
NM_000128.4(F11):c.1853T>G (p.Ile618Ser)
|
rs281875276
|
0.00002
|
NM_000128.4(F11):c.100G>C (p.Asp34His)
|
rs281875267
|
0.00001
|
NM_000128.4(F11):c.1021G>A (p.Glu341Lys)
|
rs281875270
|
0.00001
|
NM_000128.4(F11):c.1178C>T (p.Ala393Val)
|
rs547842083
|
0.00001
|
NM_000128.4(F11):c.1207G>A (p.Val403Met)
|
rs281875266
|
0.00001
|
NM_000128.4(F11):c.137G>T (p.Cys46Phe)
|
rs281875271
|
0.00001
|
NM_000128.4(F11):c.1517A>G (p.Asp506Gly)
|
rs281875258
|
0.00001
|
NM_000128.4(F11):c.1578C>G (p.Asp526Glu)
|
rs281875263
|
0.00001
|
NM_000128.4(F11):c.1693G>A (p.Glu565Lys)
|
rs281875275
|
0.00001
|
NM_000128.4(F11):c.1789G>A (p.Glu597Lys)
|
rs281875251
|
0.00001
|
NM_000128.4(F11):c.188C>T (p.Ala63Val)
|
rs281875244
|
0.00001
|
NM_000128.4(F11):c.302A>G (p.Lys101Arg)
|
rs281875272
|
0.00001
|
NM_000128.4(F11):c.419G>A (p.Cys140Tyr)
|
rs281875256
|
0.00001
|
NM_000128.4(F11):c.959T>C (p.Leu320Pro)
|
rs281875268
|
0.00001
|
NM_000128.4(F11):c.965C>T (p.Thr322Ile)
|
rs281875269
|
0.00001
|
NM_000128.4(F11):c.1079T>C (p.Leu360Pro)
|
rs281875254
|
|
NM_000128.4(F11):c.1201T>C (p.Trp401Arg)
|
rs281875262
|
|
NM_000128.4(F11):c.1361T>A (p.Ile454Lys)
|
rs281875241
|
|
NM_000128.4(F11):c.1442T>G (p.Ile481Ser)
|
rs281875242
|
|
NM_000128.4(F11):c.1507T>C (p.Ser503Pro)
|
rs140068026
|
|
NM_000128.4(F11):c.151A>C (p.Thr51Pro)
|
rs281875243
|
|
NM_000128.4(F11):c.152C>T (p.Thr51Ile)
|
rs281875252
|
|
NM_000128.4(F11):c.1531T>C (p.Tyr511His)
|
rs281875278
|
|
NM_000128.4(F11):c.1541G>T (p.Cys514Phe)
|
rs281875249
|
|
NM_000128.4(F11):c.159C>A (p.His53Gln)
|
rs281875261
|
|
NM_000128.4(F11):c.1822T>C (p.Tyr608His)
|
rs281875255
|
|
NM_000128.4(F11):c.452A>G (p.Tyr151Cys)
|
rs281875273
|
|
NM_000128.4(F11):c.664G>T (p.Asp222Tyr)
|
rs281875245
|
|
NM_000128.4(F11):c.738G>C (p.Trp246Cys)
|
rs281875279
|
|
NM_000128.4(F11):c.755G>C (p.Arg252Thr)
|
rs281875260
|
|
NM_000128.4(F11):c.764G>A (p.Cys255Tyr)
|
rs281875277
|
|
NM_000128.4(F11):c.788G>A (p.Gly263Glu)
|
rs281875274
|
|
NM_000128.4(F11):c.827C>G (p.Ser276Cys)
|
rs281875247
|
|
NM_000128.4(F11):c.830G>A (p.Gly277Asp)
|
rs281875248
|
|
NM_000128.4(F11):c.94G>A (p.Gly32Arg)
|
rs281875259
|
|
NM_000128.4(F11):c.992C>T (p.Thr331Ile)
|
rs281875253
|
|