ENST00000356592.8:c.1360T>A
|
|
|
ENST00000361925.9:c.1455T>A
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ENSP00000354651.5:p.Ala485=
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ENST00000523372.2:c.1418T>A
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|
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ENST00000638253.1:n.613T>A
|
|
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ENST00000638552.1:c.1050T>A
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ENSP00000491763.1:p.Ala350=
|
|
ENST00000638660.1:c.1074T>A
|
ENSP00000492869.1:p.Ala358=
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ENST00000638772.1:c.*3956T>A
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ENSP00000491557.1:n.*3956T>A
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ENST00000638877.1:c.1236T>A
|
|
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ENST00000639046.1:c.726T>A
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ENSP00000492659.1:p.Ala242=
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ENST00000639111.2:c.1335T>A
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ENSP00000492125.2:p.Ala445=
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ENST00000639213.2:c.1359T>A
MANE Select
|
ENSP00000491909.2:p.Ala453=
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ENST00000639278.1:c.2022T>A
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ENSP00000491958.1:n.2022T>A
|
|
ENST00000639384.1:c.*1540T>A
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ENSP00000491240.1:n.*1540T>A
|
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ENST00000639424.1:c.*559T>A
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ENSP00000491245.1:n.*559T>A
|
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ENST00000639683.1:c.1293T>A
|
ENSP00000492581.1:p.Ala431=
|
|
ENST00000639975.1:c.1269T>A
|
ENSP00000492096.1:p.Ala423=
|
|
ENST00000640500.1:n.633T>A
|
|
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ENST00000640739.1:n.6306T>A
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ENST00000640910.1:c.797T>A
|
|
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ENST00000640985.1:c.1272T>A
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ENSP00000492293.1:p.Ala424=
|
|
ENST00000641017.1:c.1428T>A
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ENSP00000493461.1:p.Ala476=
|
|
ENST00000356592.7:c.1359T>A
|
ENSP00000349000.3:p.Ala453=
|
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ENST00000361925.8:c.1335T>A
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ENSP00000354651.4:p.Ala445=
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|
ENST00000414552.6:c.1479T>A
|
ENSP00000410732.2:p.Ala493=
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|
ENST00000522990.5:c.*937T>A
|
ENSP00000430732.1:n.*937T>A
|
|
ENST00000523372.1:c.1456T>A
|
ENSP00000430124.1:n.1456T>A
|
|
NM_000816.3:c.1335T>A
|
NP_000807.2:p.Ala445=
|
|
NM_198903.2:c.1479T>A
|
NP_944493.2:p.Ala493=
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|
NM_198904.2:c.1359T>A
|
NP_944494.1:p.Ala453=
|
|
NM_001375339.1:c.1350T>A
|
NP_001362268.1:p.Ala450=
|
|
NM_001375340.1:c.*193T>A
|
NP_001362269.1:n.*193T>A
|
|
NM_001375341.1:c.1356T>A
|
NP_001362270.1:p.Ala452=
|
|
NM_001375342.1:c.1332T>A
|
NP_001362271.1:p.Ala444=
|
|
NM_001375343.1:c.1455T>A
|
NP_001362272.1:p.Ala485=
|
|
NM_001375344.1:c.1398T>A
|
NP_001362273.1:p.Ala466=
|
|
NM_001375345.1:c.1269T>A
|
NP_001362274.1:p.Ala423=
|
|
NM_001375346.1:c.1293T>A
|
NP_001362275.1:p.Ala431=
|
|
NM_001375347.1:c.1272T>A
|
NP_001362276.1:p.Ala424=
|
|
NM_001375348.1:c.915T>A
|
NP_001362277.1:p.Ala305=
|
|
NM_001375349.1:c.1050T>A
|
NP_001362278.1:p.Ala350=
|
|
NM_001375350.1:c.939T>A
|
NP_001362279.1:p.Ala313=
|
|
NM_198904.3:c.1359T>A
|
NP_944494.1:p.Ala453=
|
|
NM_198904.4:c.1359T>A
MANE Select
|
NP_944494.1:p.Ala453=
|
|