NM_001114753.3(ENG):c.179C>A (p.Ala60Asp)
|
rs146100407
|
0.00117
|
NM_001114753.3(ENG):c.-9G>A
|
rs368423516
|
0.00040
|
NM_001114753.3(ENG):c.7C>T (p.Arg3Cys)
|
rs139334561
|
0.00024
|
NM_001114753.3(ENG):c.1015G>A (p.Ala339Thr)
|
rs761463410
|
0.00008
|
NM_001114753.3(ENG):c.-126G>A
|
rs940261789
|
0.00005
|
NM_001114753.3(ENG):c.1067T>A (p.Met356Lys)
|
rs138190783
|
0.00003
|
NM_001114753.3(ENG):c.1058A>G (p.Glu353Gly)
|
rs868730895
|
0.00001
|
NM_001114753.3(ENG):c.158G>A (p.Cys53Tyr)
|
rs187643086
|
0.00001
|
NM_001114753.3(ENG):c.1850C>T (p.Thr617Met)
|
rs201031046
|
0.00001
|
NM_001114753.3(ENG):c.1955G>A (p.Cys652Tyr)
|
rs774869649
|
0.00001
|
NM_001114753.3(ENG):c.1970T>C (p.Met657Thr)
|
rs768873662
|
0.00001
|
NM_001114753.3(ENG):c.68-17G>A
|
rs570198729
|
0.00001
|
NM_001114753.3(ENG):c.911G>A (p.Arg304Gln)
|
rs753429934
|
0.00001
|
NM_001114753.3(ENG):c.-2G>A
|
|
|
NM_001114753.3(ENG):c.-79C>T
|
rs1564466502
|
|
NM_001114753.3(ENG):c.1018C>T (p.Pro340Ser)
|
rs773463077
|
|
NM_001114753.3(ENG):c.1076T>G (p.Ile359Ser)
|
|
|
NM_001114753.3(ENG):c.1089T>G (p.Cys363Trp)
|
rs777177134
|
|
NM_001114753.3(ENG):c.1099G>C (p.Ala367Pro)
|
rs372371435
|
|
NM_001114753.3(ENG):c.137C>T (p.Thr46Ile)
|
rs1393437924
|
|
NM_001114753.3(ENG):c.182T>C (p.Ile61Thr)
|
|
|
NM_001114753.3(ENG):c.1852+21_1852+22del
|
|
|
NM_001114753.3(ENG):c.360+6T>G
|
rs2131894931
|
|
NM_001114753.3(ENG):c.411G>T (p.Glu137Asp)
|
|
|
NM_001114753.3(ENG):c.497A>C (p.Gln166Pro)
|
rs994887264
|
|
NM_001114753.3(ENG):c.512G>C (p.Arg171Pro)
|
rs756980265
|
|
NM_001114753.3(ENG):c.569T>A (p.Met190Lys)
|
rs1830602163
|
|
NM_001114753.3(ENG):c.578C>T (p.Thr193Met)
|
rs775442178
|
|
NM_001114753.3(ENG):c.581T>C (p.Leu194Pro)
|
rs2131889364
|
|
NM_001114753.3(ENG):c.583G>A (p.Glu195Lys)
|
rs1255912441
|
|
NM_001114753.3(ENG):c.67+4G>A
|
rs1309975584
|
|
NM_001114753.3(ENG):c.67+5G>A
|
rs763111216
|
|
NM_001114753.3(ENG):c.706_708del (p.Val236del)
|
rs1064794221
|
|
NM_001114753.3(ENG):c.713T>A (p.Val238Glu)
|
rs1060501415
|
|
NM_001114753.3(ENG):c.742G>C (p.Asp248His)
|
|
|
NM_001114753.3(ENG):c.742_743insT (p.Asp248fs)
|
rs1213847963
|
|
NM_001114753.3(ENG):c.758T>C (p.Leu253Pro)
|
rs2131887841
|
|
NM_001114753.3(ENG):c.764G>T (p.Gly255Val)
|
rs2131887828
|
|
NM_001114753.3(ENG):c.788T>A (p.Ile263Asn)
|
rs1085307431
|
|
NM_001114753.3(ENG):c.933_968del (p.Ala312_Val323del)
|
rs2131886859
|
|
NM_001114753.3(ENG):c.98A>C (p.Gln33Pro)
|
rs863223531
|
|