ENST00000356592.8:c.1167A>C
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ENST00000361925.9:c.1262A>C
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ENSP00000354651.5:p.Asp421Ala
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ENST00000523372.2:c.1225A>C
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ENST00000638253.1:n.420A>C
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ENST00000638552.1:c.857A>C
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ENSP00000491763.1:p.Asp286Ala
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ENST00000638660.1:c.881A>C
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ENSP00000492869.1:p.Asp294Ala
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ENST00000638772.1:c.*3763A>C
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ENSP00000491557.1:n.*3763A>C
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ENST00000638877.1:c.1043A>C
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ENST00000639046.1:c.533A>C
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ENSP00000492659.1:p.Asp178Ala
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ENST00000639111.2:c.1142A>C
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ENSP00000492125.2:p.Asp381Ala
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ENST00000639213.2:c.1166A>C
MANE Select
|
ENSP00000491909.2:p.Asp389Ala
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ENST00000639278.1:c.1829A>C
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ENSP00000491958.1:n.1829A>C
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ENST00000639384.1:c.*1347A>C
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ENSP00000491240.1:n.*1347A>C
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ENST00000639424.1:c.*366A>C
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ENSP00000491245.1:n.*366A>C
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ENST00000639683.1:c.1100A>C
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ENSP00000492581.1:p.Asp367Ala
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ENST00000639975.1:c.1076A>C
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ENSP00000492096.1:p.Asp359Ala
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ENST00000640500.1:n.440A>C
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ENST00000640739.1:n.6113A>C
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ENST00000640910.1:c.604A>C
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ENST00000640985.1:c.1079A>C
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ENSP00000492293.1:p.Asp360Ala
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ENST00000641017.1:c.1235A>C
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ENSP00000493461.1:p.Asp412Ala
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ENST00000356592.7:c.1166A>C
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ENSP00000349000.3:p.Asp389Ala
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ENST00000361925.8:c.1142A>C
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ENSP00000354651.4:p.Asp381Ala
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ENST00000414552.6:c.1286A>C
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ENSP00000410732.2:p.Asp429Ala
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ENST00000522990.5:c.*744A>C
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ENSP00000430732.1:n.*744A>C
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ENST00000523372.1:c.1263A>C
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ENSP00000430124.1:n.1263A>C
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NM_000816.3:c.1142A>C
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NP_000807.2:p.Asp381Ala
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NM_198903.2:c.1286A>C
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NP_944493.2:p.Asp429Ala
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NM_198904.2:c.1166A>C
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NP_944494.1:p.Asp389Ala
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NM_001375339.1:c.1157A>C
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NP_001362268.1:p.Asp386Ala
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NM_001375340.1:c.960A>C
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NP_001362269.1:p.Ter320Cys
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NM_001375341.1:c.1163A>C
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NP_001362270.1:p.Asp388Ala
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NM_001375342.1:c.1139A>C
|
NP_001362271.1:p.Asp380Ala
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NM_001375343.1:c.1262A>C
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NP_001362272.1:p.Asp421Ala
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|
NM_001375344.1:c.1205A>C
|
NP_001362273.1:p.Asp402Ala
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NM_001375345.1:c.1076A>C
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NP_001362274.1:p.Asp359Ala
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NM_001375346.1:c.1100A>C
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NP_001362275.1:p.Asp367Ala
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NM_001375347.1:c.1079A>C
|
NP_001362276.1:p.Asp360Ala
|
|
NM_001375348.1:c.722A>C
|
NP_001362277.1:p.Asp241Ala
|
|
NM_001375349.1:c.857A>C
|
NP_001362278.1:p.Asp286Ala
|
|
NM_001375350.1:c.746A>C
|
NP_001362279.1:p.Asp249Ala
|
|
NM_198904.3:c.1166A>C
|
NP_944494.1:p.Asp389Ala
|
|
NM_198904.4:c.1166A>C
MANE Select
|
NP_944494.1:p.Asp389Ala
|
|