ENST00000350026.11:c.3906T>C
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ENSP00000055163.8:p.Ser1302=
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ENST00000414678.8:c.3975T>C
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ENSP00000412835.3:p.Ser1325=
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ENST00000637015.2:c.4194T>C
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ENSP00000489729.2:p.Ser1398=
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ENST00000346085.10:c.3945T>C
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ENSP00000344546.5:p.Ser1315=
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ENST00000350026.10:c.3657T>C
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ENSP00000055163.7:p.Ser1219=
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ENST00000414678.7:c.2223T>C
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ENSP00000412835.2:p.Ser741=
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ENST00000635849.1:c.1386T>C
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ENSP00000490948.1:p.Ser462=
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ENST00000635957.1:c.1017T>C
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ENSP00000490385.1:p.Ser339=
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ENST00000636930.2:c.4065T>C
MANE Select
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ENSP00000490491.2:p.Ser1355=
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ENST00000636940.1:n.2062T>C
|
|
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ENST00000637015.1:c.1433T>C
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ENST00000637568.1:c.1347T>C
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|
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ENST00000637741.1:n.731T>C
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ENST00000637810.1:c.1407T>C
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ENSP00000489636.1:p.Ser469=
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ENST00000637904.1:c.1566T>C
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ENSP00000490550.1:p.Ser522=
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ENST00000647938.1:c.3696T>C
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ENSP00000498155.1:p.Ser1232=
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ENST00000346085.9:c.3696T>C
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ENSP00000344546.4:p.Ser1232=
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ENST00000350026.9:c.3657T>C
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ENSP00000055163.7:p.Ser1219=
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ENST00000414678.6:c.2223T>C
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ENSP00000412835.2:p.Ser741=
|
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NM_017519.2:c.3657T>C
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NP_059989.2:p.Ser1219=
|
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NM_020732.3:c.3696T>C
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NP_065783.3:p.Ser1232=
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XM_005267069.3:c.3816T>C
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XP_005267126.2:p.Ser1272=
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XM_011535984.1:c.2895T>C
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XP_011534286.1:p.Ser965=
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XM_011535985.1:c.2715T>C
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XP_011534287.1:p.Ser905=
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XM_011535986.1:c.2475T>C
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XP_011534288.1:p.Ser825=
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XM_011535987.1:c.2094T>C
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XP_011534289.1:p.Ser698=
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XM_011535988.1:c.957T>C
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XP_011534290.1:p.Ser319=
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NM_001346813.1:c.3816T>C
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NP_001333742.1:p.Ser1272=
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NM_001363725.1:c.1566T>C
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NP_001350654.1:p.Ser522=
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XM_011535984.2:c.4026T>C
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XP_011534286.2:p.Ser1342=
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XM_011535988.3:c.957T>C
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XP_011534290.1:p.Ser319=
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XM_017011103.2:c.3927T>C
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XP_016866592.1:p.Ser1309=
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XM_017011104.1:c.3897T>C
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XP_016866593.1:p.Ser1299=
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XM_017011105.2:c.3867T>C
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XP_016866594.1:p.Ser1289=
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XM_017011106.2:c.3738T>C
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XP_016866595.1:p.Ser1246=
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XM_017011107.2:c.3717T>C
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XP_016866596.1:p.Ser1239=
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XR_002956289.1:n.4109T>C
|
|
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NM_001363725.2:c.1566T>C
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NP_001350654.1:p.Ser522=
|
|
NM_001371656.1:c.3945T>C
|
NP_001358585.1:p.Ser1315=
|
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NM_001374820.1:c.3945T>C
|
NP_001361749.1:p.Ser1315=
|
|
NM_001374828.1:c.4065T>C
MANE Select
|
NP_001361757.1:p.Ser1355=
|
|
NM_017519.3:c.3906T>C
|
NP_059989.3:p.Ser1302=
|
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