ENST00000356592.8:c.1401T>C
|
|
|
ENST00000361925.9:c.1496T>C
|
ENSP00000354651.5:p.Val499Ala
|
|
ENST00000523372.2:c.1459T>C
|
|
|
ENST00000638253.1:n.654T>C
|
|
|
ENST00000638552.1:c.1091T>C
|
ENSP00000491763.1:p.Val364Ala
|
|
ENST00000638660.1:c.1115T>C
|
ENSP00000492869.1:p.Val372Ala
|
|
ENST00000638772.1:c.*3997T>C
|
ENSP00000491557.1:n.*3997T>C
|
|
ENST00000638877.1:c.1277T>C
|
|
|
ENST00000639046.1:c.767T>C
|
ENSP00000492659.1:p.Val256Ala
|
|
ENST00000639111.2:c.1376T>C
|
ENSP00000492125.2:p.Val459Ala
|
|
ENST00000639213.2:c.1400T>C
MANE Select
|
ENSP00000491909.2:p.Val467Ala
|
|
ENST00000639278.1:c.2063T>C
|
ENSP00000491958.1:n.2063T>C
|
|
ENST00000639384.1:c.*1581T>C
|
ENSP00000491240.1:n.*1581T>C
|
|
ENST00000639424.1:c.*600T>C
|
ENSP00000491245.1:n.*600T>C
|
|
ENST00000639683.1:c.1334T>C
|
ENSP00000492581.1:p.Val445Ala
|
|
ENST00000639975.1:c.1310T>C
|
ENSP00000492096.1:p.Val437Ala
|
|
ENST00000640500.1:n.674T>C
|
|
|
ENST00000640739.1:n.6347T>C
|
|
|
ENST00000640910.1:c.838T>C
|
|
|
ENST00000640985.1:c.1313T>C
|
ENSP00000492293.1:p.Val438Ala
|
|
ENST00000641017.1:c.1469T>C
|
ENSP00000493461.1:p.Val490Ala
|
|
ENST00000356592.7:c.1400T>C
|
ENSP00000349000.3:p.Val467Ala
|
|
ENST00000361925.8:c.1376T>C
|
ENSP00000354651.4:p.Val459Ala
|
|
ENST00000414552.6:c.1520T>C
|
ENSP00000410732.2:p.Val507Ala
|
|
ENST00000522990.5:c.*978T>C
|
ENSP00000430732.1:n.*978T>C
|
|
ENST00000523372.1:c.1497T>C
|
ENSP00000430124.1:n.1497T>C
|
|
NM_000816.3:c.1376T>C
|
NP_000807.2:p.Val459Ala
|
|
NM_198903.2:c.1520T>C
|
NP_944493.2:p.Val507Ala
|
|
NM_198904.2:c.1400T>C
|
NP_944494.1:p.Val467Ala
|
|
NM_001375339.1:c.1391T>C
|
NP_001362268.1:p.Val464Ala
|
|
NM_001375340.1:c.*234T>C
|
NP_001362269.1:n.*234T>C
|
|
NM_001375341.1:c.1397T>C
|
NP_001362270.1:p.Val466Ala
|
|
NM_001375342.1:c.1373T>C
|
NP_001362271.1:p.Val458Ala
|
|
NM_001375343.1:c.1496T>C
|
NP_001362272.1:p.Val499Ala
|
|
NM_001375344.1:c.1439T>C
|
NP_001362273.1:p.Val480Ala
|
|
NM_001375345.1:c.1310T>C
|
NP_001362274.1:p.Val437Ala
|
|
NM_001375346.1:c.1334T>C
|
NP_001362275.1:p.Val445Ala
|
|
NM_001375347.1:c.1313T>C
|
NP_001362276.1:p.Val438Ala
|
|
NM_001375348.1:c.956T>C
|
NP_001362277.1:p.Val319Ala
|
|
NM_001375349.1:c.1091T>C
|
NP_001362278.1:p.Val364Ala
|
|
NM_001375350.1:c.980T>C
|
NP_001362279.1:p.Val327Ala
|
|
NM_198904.3:c.1400T>C
|
NP_944494.1:p.Val467Ala
|
|
NM_198904.4:c.1400T>C
MANE Select
|
NP_944494.1:p.Val467Ala
|
|