ENST00000356592.8:c.1381C>G
|
|
|
ENST00000361925.9:c.1476C>G
|
ENSP00000354651.5:p.Ala492=
|
|
ENST00000523372.2:c.1439C>G
|
|
|
ENST00000638253.1:n.634C>G
|
|
|
ENST00000638552.1:c.1071C>G
|
ENSP00000491763.1:p.Ala357=
|
|
ENST00000638660.1:c.1095C>G
|
ENSP00000492869.1:p.Ala365=
|
|
ENST00000638772.1:c.*3977C>G
|
ENSP00000491557.1:n.*3977C>G
|
|
ENST00000638877.1:c.1257C>G
|
|
|
ENST00000639046.1:c.747C>G
|
ENSP00000492659.1:p.Ala249=
|
|
ENST00000639111.2:c.1356C>G
|
ENSP00000492125.2:p.Ala452=
|
|
ENST00000639213.2:c.1380C>G
MANE Select
|
ENSP00000491909.2:p.Ala460=
|
|
ENST00000639278.1:c.2043C>G
|
ENSP00000491958.1:n.2043C>G
|
|
ENST00000639384.1:c.*1561C>G
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ENSP00000491240.1:n.*1561C>G
|
|
ENST00000639424.1:c.*580C>G
|
ENSP00000491245.1:n.*580C>G
|
|
ENST00000639683.1:c.1314C>G
|
ENSP00000492581.1:p.Ala438=
|
|
ENST00000639975.1:c.1290C>G
|
ENSP00000492096.1:p.Ala430=
|
|
ENST00000640500.1:n.654C>G
|
|
|
ENST00000640739.1:n.6327C>G
|
|
|
ENST00000640910.1:c.818C>G
|
|
|
ENST00000640985.1:c.1293C>G
|
ENSP00000492293.1:p.Ala431=
|
|
ENST00000641017.1:c.1449C>G
|
ENSP00000493461.1:p.Ala483=
|
|
ENST00000356592.7:c.1380C>G
|
ENSP00000349000.3:p.Ala460=
|
|
ENST00000361925.8:c.1356C>G
|
ENSP00000354651.4:p.Ala452=
|
|
ENST00000414552.6:c.1500C>G
|
ENSP00000410732.2:p.Ala500=
|
|
ENST00000522990.5:c.*958C>G
|
ENSP00000430732.1:n.*958C>G
|
|
ENST00000523372.1:c.1477C>G
|
ENSP00000430124.1:n.1477C>G
|
|
NM_000816.3:c.1356C>G
|
NP_000807.2:p.Ala452=
|
|
NM_198903.2:c.1500C>G
|
NP_944493.2:p.Ala500=
|
|
NM_198904.2:c.1380C>G
|
NP_944494.1:p.Ala460=
|
|
NM_001375339.1:c.1371C>G
|
NP_001362268.1:p.Ala457=
|
|
NM_001375340.1:c.*214C>G
|
NP_001362269.1:n.*214C>G
|
|
NM_001375341.1:c.1377C>G
|
NP_001362270.1:p.Ala459=
|
|
NM_001375342.1:c.1353C>G
|
NP_001362271.1:p.Ala451=
|
|
NM_001375343.1:c.1476C>G
|
NP_001362272.1:p.Ala492=
|
|
NM_001375344.1:c.1419C>G
|
NP_001362273.1:p.Ala473=
|
|
NM_001375345.1:c.1290C>G
|
NP_001362274.1:p.Ala430=
|
|
NM_001375346.1:c.1314C>G
|
NP_001362275.1:p.Ala438=
|
|
NM_001375347.1:c.1293C>G
|
NP_001362276.1:p.Ala431=
|
|
NM_001375348.1:c.936C>G
|
NP_001362277.1:p.Ala312=
|
|
NM_001375349.1:c.1071C>G
|
NP_001362278.1:p.Ala357=
|
|
NM_001375350.1:c.960C>G
|
NP_001362279.1:p.Ala320=
|
|
NM_198904.3:c.1380C>G
|
NP_944494.1:p.Ala460=
|
|
NM_198904.4:c.1380C>G
MANE Select
|
NP_944494.1:p.Ala460=
|
|