ENST00000356592.8:c.1400G=
|
|
|
ENST00000361925.9:c.1495G=
|
ENSP00000354651.5:p.Val499=
|
|
ENST00000523372.2:c.1458G=
|
|
|
ENST00000638253.1:n.653G=
|
|
|
ENST00000638552.1:c.1090G=
|
ENSP00000491763.1:p.Val364=
|
|
ENST00000638660.1:c.1114G=
|
ENSP00000492869.1:p.Val372=
|
|
ENST00000638772.1:c.*3996G=
|
ENSP00000491557.1:n.*3996G=
|
|
ENST00000638877.1:c.1276G=
|
|
|
ENST00000639046.1:c.766G=
|
ENSP00000492659.1:p.Val256=
|
|
ENST00000639111.2:c.1375G=
|
ENSP00000492125.2:p.Val459=
|
|
ENST00000639213.2:c.1399G=
MANE Select
|
ENSP00000491909.2:p.Val467=
|
|
ENST00000639278.1:c.2062G=
|
ENSP00000491958.1:n.2062G=
|
|
ENST00000639384.1:c.*1580G=
|
ENSP00000491240.1:n.*1580G=
|
|
ENST00000639424.1:c.*599G=
|
ENSP00000491245.1:n.*599G=
|
|
ENST00000639683.1:c.1333G=
|
ENSP00000492581.1:p.Val445=
|
|
ENST00000639975.1:c.1309G=
|
ENSP00000492096.1:p.Val437=
|
|
ENST00000640500.1:n.673G=
|
|
|
ENST00000640739.1:n.6346G=
|
|
|
ENST00000640910.1:c.837G=
|
|
|
ENST00000640985.1:c.1312G=
|
ENSP00000492293.1:p.Val438=
|
|
ENST00000641017.1:c.1468G=
|
ENSP00000493461.1:p.Val490=
|
|
ENST00000356592.7:c.1399G=
|
ENSP00000349000.3:p.Val467=
|
|
ENST00000361925.8:c.1375G=
|
ENSP00000354651.4:p.Val459=
|
|
ENST00000414552.6:c.1519G=
|
ENSP00000410732.2:p.Val507=
|
|
ENST00000522990.5:c.*977G=
|
ENSP00000430732.1:n.*977G=
|
|
ENST00000523372.1:c.1496G=
|
ENSP00000430124.1:n.1496G=
|
|
NM_000816.3:c.1375G=
|
NP_000807.2:p.Val459=
|
|
NM_198903.2:c.1519G=
|
NP_944493.2:p.Val507=
|
|
NM_198904.2:c.1399G=
|
NP_944494.1:p.Val467=
|
|
NM_001375339.1:c.1390G=
|
NP_001362268.1:p.Val464=
|
|
NM_001375340.1:c.*233G=
|
NP_001362269.1:n.*233G=
|
|
NM_001375341.1:c.1396G=
|
NP_001362270.1:p.Val466=
|
|
NM_001375342.1:c.1372G=
|
NP_001362271.1:p.Val458=
|
|
NM_001375343.1:c.1495G=
|
NP_001362272.1:p.Val499=
|
|
NM_001375344.1:c.1438G=
|
NP_001362273.1:p.Val480=
|
|
NM_001375345.1:c.1309G=
|
NP_001362274.1:p.Val437=
|
|
NM_001375346.1:c.1333G=
|
NP_001362275.1:p.Val445=
|
|
NM_001375347.1:c.1312G=
|
NP_001362276.1:p.Val438=
|
|
NM_001375348.1:c.955G=
|
NP_001362277.1:p.Val319=
|
|
NM_001375349.1:c.1090G=
|
NP_001362278.1:p.Val364=
|
|
NM_001375350.1:c.979G=
|
NP_001362279.1:p.Val327=
|
|
NM_198904.3:c.1399G=
|
NP_944494.1:p.Val467=
|
|
NM_198904.4:c.1399G=
MANE Select
|
NP_944494.1:p.Val467=
|
|