ENST00000356592.8:c.1351C>A
|
|
|
ENST00000361925.9:c.1446C>A
|
ENSP00000354651.5:p.Asp482Glu
|
|
ENST00000523372.2:c.1409C>A
|
|
|
ENST00000638253.1:n.604C>A
|
|
|
ENST00000638552.1:c.1041C>A
|
ENSP00000491763.1:p.Asp347Glu
|
|
ENST00000638660.1:c.1065C>A
|
ENSP00000492869.1:p.Asp355Glu
|
|
ENST00000638772.1:c.*3947C>A
|
ENSP00000491557.1:n.*3947C>A
|
|
ENST00000638877.1:c.1227C>A
|
|
|
ENST00000639046.1:c.717C>A
|
ENSP00000492659.1:p.Asp239Glu
|
|
ENST00000639111.2:c.1326C>A
|
ENSP00000492125.2:p.Asp442Glu
|
|
ENST00000639213.2:c.1350C>A
MANE Select
|
ENSP00000491909.2:p.Asp450Glu
|
|
ENST00000639278.1:c.2013C>A
|
ENSP00000491958.1:n.2013C>A
|
|
ENST00000639384.1:c.*1531C>A
|
ENSP00000491240.1:n.*1531C>A
|
|
ENST00000639424.1:c.*550C>A
|
ENSP00000491245.1:n.*550C>A
|
|
ENST00000639683.1:c.1284C>A
|
ENSP00000492581.1:p.Asp428Glu
|
|
ENST00000639975.1:c.1260C>A
|
ENSP00000492096.1:p.Asp420Glu
|
|
ENST00000640500.1:n.624C>A
|
|
|
ENST00000640739.1:n.6297C>A
|
|
|
ENST00000640910.1:c.788C>A
|
|
|
ENST00000640985.1:c.1263C>A
|
ENSP00000492293.1:p.Asp421Glu
|
|
ENST00000641017.1:c.1419C>A
|
ENSP00000493461.1:p.Asp473Glu
|
|
ENST00000356592.7:c.1350C>A
|
ENSP00000349000.3:p.Asp450Glu
|
|
ENST00000361925.8:c.1326C>A
|
ENSP00000354651.4:p.Asp442Glu
|
|
ENST00000414552.6:c.1470C>A
|
ENSP00000410732.2:p.Asp490Glu
|
|
ENST00000522990.5:c.*928C>A
|
ENSP00000430732.1:n.*928C>A
|
|
ENST00000523372.1:c.1447C>A
|
ENSP00000430124.1:n.1447C>A
|
|
NM_000816.3:c.1326C>A
|
NP_000807.2:p.Asp442Glu
|
|
NM_198903.2:c.1470C>A
|
NP_944493.2:p.Asp490Glu
|
|
NM_198904.2:c.1350C>A
|
NP_944494.1:p.Asp450Glu
|
|
NM_001375339.1:c.1341C>A
|
NP_001362268.1:p.Asp447Glu
|
|
NM_001375340.1:c.*184C>A
|
NP_001362269.1:n.*184C>A
|
|
NM_001375341.1:c.1347C>A
|
NP_001362270.1:p.Asp449Glu
|
|
NM_001375342.1:c.1323C>A
|
NP_001362271.1:p.Asp441Glu
|
|
NM_001375343.1:c.1446C>A
|
NP_001362272.1:p.Asp482Glu
|
|
NM_001375344.1:c.1389C>A
|
NP_001362273.1:p.Asp463Glu
|
|
NM_001375345.1:c.1260C>A
|
NP_001362274.1:p.Asp420Glu
|
|
NM_001375346.1:c.1284C>A
|
NP_001362275.1:p.Asp428Glu
|
|
NM_001375347.1:c.1263C>A
|
NP_001362276.1:p.Asp421Glu
|
|
NM_001375348.1:c.906C>A
|
NP_001362277.1:p.Asp302Glu
|
|
NM_001375349.1:c.1041C>A
|
NP_001362278.1:p.Asp347Glu
|
|
NM_001375350.1:c.930C>A
|
NP_001362279.1:p.Asp310Glu
|
|
NM_198904.3:c.1350C>A
|
NP_944494.1:p.Asp450Glu
|
|
NM_198904.4:c.1350C>A
MANE Select
|
NP_944494.1:p.Asp450Glu
|
|