NM_001354712.2(THRB):c.1029T>G (p.Asn343Lys)
|
rs1354053223
|
0.00001
|
NM_001354712.2(THRB):c.1148G>A (p.Arg383His)
|
rs121918708
|
0.00001
|
NM_001354712.2(THRB):c.1286G>A (p.Arg429Gln)
|
rs1553609210
|
0.00001
|
NM_001354712.2(THRB):c.1312C>T (p.Arg438Cys)
|
rs367757240
|
0.00001
|
NM_001354712.2(THRB):c.1313G>A (p.Arg438His)
|
rs121918698
|
0.00001
|
NM_001354712.2(THRB):c.1357C>G (p.Pro453Ala)
|
rs28933408
|
0.00001
|
NM_001354712.2(THRB):c.1010_1012del (p.Thr337del)
|
rs387906515
|
|
NM_001354712.2(THRB):c.1012C>T (p.Arg338Trp)
|
rs121918697
|
|
NM_001354712.2(THRB):c.1020G>C (p.Gln340His)
|
rs121918688
|
|
NM_001354712.2(THRB):c.1031G>A (p.Gly344Glu)
|
rs1553610974
|
|
NM_001354712.2(THRB):c.1033G>A (p.Gly345Ser)
|
rs121918686
|
|
NM_001354712.2(THRB):c.1033G>C (p.Gly345Arg)
|
rs121918686
|
|
NM_001354712.2(THRB):c.1034G>T (p.Gly345Val)
|
rs28999970
|
|
NM_001354712.2(THRB):c.1040G>A (p.Gly347Glu)
|
rs28999971
|
|
NM_001354712.2(THRB):c.1302C>A (p.Cys434Ter)
|
rs121918705
|
|
NM_001354712.2(THRB):c.1305T>G (p.His435Gln)
|
rs1553609185
|
|
NM_001354712.2(THRB):c.1312del (p.Arg438fs)
|
rs1553609179
|
|
NM_001354712.2(THRB):c.1324A>G (p.Met442Val)
|
rs121918691
|
|
NM_001354712.2(THRB):c.1326_1327delinsAT (p.Met442_Lys443delinsIleTer)
|
rs1553609167
|
|
NM_001354712.2(THRB):c.1327A>G (p.Lys443Glu)
|
rs121918692
|
|
NM_001354712.2(THRB):c.1336T>C (p.Cys446Arg)
|
rs121918703
|
|
NM_001354712.2(THRB):c.1341dup (p.Thr448fs)
|
|
|
NM_001354712.2(THRB):c.1348C>T (p.Leu450Phe)
|
rs1553609152
|
|
NM_001354712.2(THRB):c.1357C>A (p.Pro453Thr)
|
rs28933408
|
|
NM_001354712.2(THRB):c.1357C>T (p.Pro453Ser)
|
rs28933408
|
|
NM_001354712.2(THRB):c.1358C>A (p.Pro453His)
|
rs121918687
|
|
NM_001354712.2(THRB):c.1358dup (p.Leu454fs)
|
rs1553609119
|
|
NM_001354712.2(THRB):c.1373T>C (p.Val458Ala)
|
rs121918704
|
|
NM_001354712.2(THRB):c.1378G>A (p.Glu460Lys)
|
rs1553609090
|
|
NM_001354712.2(THRB):c.803C>G (p.Ala268Gly)
|
rs750905761
|
|
NM_001354712.2(THRB):c.928A>G (p.Met310Val)
|
rs1553611094
|
|
NM_001354712.2(THRB):c.938T>C (p.Met313Thr)
|
rs1553611083
|
|
NM_001354712.2(THRB):c.941C>T (p.Ser314Phe)
|
rs1553611075
|
|
NM_001354712.2(THRB):c.947G>A (p.Arg316His)
|
rs121918695
|
|
NM_001354712.2(THRB):c.949G>A (p.Ala317Thr)
|
rs121918690
|
|
NM_001354712.2(THRB):c.958C>T (p.Arg320Cys)
|
rs121918696
|
|
NM_001354712.2(THRB):c.959G>A (p.Arg320His)
|
rs121918693
|
|
NM_001354712.2(THRB):c.980C>A (p.Thr327Asn)
|
rs1553611038
|
|
NM_001354712.2(THRB):c.994G>A (p.Gly332Arg)
|
rs28999969
|
|