ENST00000356592.8:c.1303A>C
|
|
|
ENST00000361925.9:c.1398A>C
|
ENSP00000354651.5:p.Thr466=
|
|
ENST00000523372.2:c.1361A>C
|
|
|
ENST00000638253.1:n.556A>C
|
|
|
ENST00000638552.1:c.993A>C
|
ENSP00000491763.1:p.Thr331=
|
|
ENST00000638660.1:c.1017A>C
|
ENSP00000492869.1:p.Thr339=
|
|
ENST00000638772.1:c.*3899A>C
|
ENSP00000491557.1:n.*3899A>C
|
|
ENST00000638877.1:c.1179A>C
|
|
|
ENST00000639046.1:c.669A>C
|
ENSP00000492659.1:p.Thr223=
|
|
ENST00000639111.2:c.1278A>C
|
ENSP00000492125.2:p.Thr426=
|
|
ENST00000639213.2:c.1302A>C
MANE Select
|
ENSP00000491909.2:p.Thr434=
|
|
ENST00000639278.1:c.1965A>C
|
ENSP00000491958.1:n.1965A>C
|
|
ENST00000639384.1:c.*1483A>C
|
ENSP00000491240.1:n.*1483A>C
|
|
ENST00000639424.1:c.*502A>C
|
ENSP00000491245.1:n.*502A>C
|
|
ENST00000639683.1:c.1236A>C
|
ENSP00000492581.1:p.Thr412=
|
|
ENST00000639975.1:c.1212A>C
|
ENSP00000492096.1:p.Thr404=
|
|
ENST00000640500.1:n.576A>C
|
|
|
ENST00000640739.1:n.6249A>C
|
|
|
ENST00000640910.1:c.740A>C
|
|
|
ENST00000640985.1:c.1215A>C
|
ENSP00000492293.1:p.Thr405=
|
|
ENST00000641017.1:c.1371A>C
|
ENSP00000493461.1:p.Thr457=
|
|
ENST00000356592.7:c.1302A>C
|
ENSP00000349000.3:p.Thr434=
|
|
ENST00000361925.8:c.1278A>C
|
ENSP00000354651.4:p.Thr426=
|
|
ENST00000414552.6:c.1422A>C
|
ENSP00000410732.2:p.Thr474=
|
|
ENST00000522990.5:c.*880A>C
|
ENSP00000430732.1:n.*880A>C
|
|
ENST00000523372.1:c.1399A>C
|
ENSP00000430124.1:n.1399A>C
|
|
NM_000816.3:c.1278A>C
|
NP_000807.2:p.Thr426=
|
|
NM_198903.2:c.1422A>C
|
NP_944493.2:p.Thr474=
|
|
NM_198904.2:c.1302A>C
|
NP_944494.1:p.Thr434=
|
|
NM_001375339.1:c.1293A>C
|
NP_001362268.1:p.Thr431=
|
|
NM_001375340.1:c.*136A>C
|
NP_001362269.1:n.*136A>C
|
|
NM_001375341.1:c.1299A>C
|
NP_001362270.1:p.Thr433=
|
|
NM_001375342.1:c.1275A>C
|
NP_001362271.1:p.Thr425=
|
|
NM_001375343.1:c.1398A>C
|
NP_001362272.1:p.Thr466=
|
|
NM_001375344.1:c.1341A>C
|
NP_001362273.1:p.Thr447=
|
|
NM_001375345.1:c.1212A>C
|
NP_001362274.1:p.Thr404=
|
|
NM_001375346.1:c.1236A>C
|
NP_001362275.1:p.Thr412=
|
|
NM_001375347.1:c.1215A>C
|
NP_001362276.1:p.Thr405=
|
|
NM_001375348.1:c.858A>C
|
NP_001362277.1:p.Thr286=
|
|
NM_001375349.1:c.993A>C
|
NP_001362278.1:p.Thr331=
|
|
NM_001375350.1:c.882A>C
|
NP_001362279.1:p.Thr294=
|
|
NM_198904.3:c.1302A>C
|
NP_944494.1:p.Thr434=
|
|
NM_198904.4:c.1302A>C
MANE Select
|
NP_944494.1:p.Thr434=
|
|