ENST00000350026.11:c.3983C>T
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ENSP00000055163.8:p.Ala1328Val
|
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ENST00000414678.8:c.4052C>T
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ENSP00000412835.3:p.Ala1351Val
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ENST00000637015.2:c.4271C>T
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ENSP00000489729.2:p.Ala1424Val
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ENST00000346085.10:c.4022C>T
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ENSP00000344546.5:p.Ala1341Val
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ENST00000350026.10:c.3734C>T
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ENSP00000055163.7:p.Ala1245Val
|
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ENST00000414678.7:c.2300C>T
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ENSP00000412835.2:p.Ala767Val
|
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ENST00000635849.1:c.1463C>T
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ENSP00000490948.1:p.Ala488Val
|
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ENST00000635957.1:c.1094C>T
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ENSP00000490385.1:p.Ala365Val
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ENST00000636930.2:c.4142C>T
MANE Select
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ENSP00000490491.2:p.Ala1381Val
|
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ENST00000636940.1:n.2139C>T
|
|
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ENST00000637015.1:c.1510C>T
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|
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ENST00000637568.1:c.1424C>T
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|
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ENST00000637741.1:n.808C>T
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|
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ENST00000637810.1:c.1484C>T
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ENSP00000489636.1:p.Ala495Val
|
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ENST00000637904.1:c.1643C>T
|
ENSP00000490550.1:p.Ala548Val
|
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ENST00000647938.1:c.3773C>T
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ENSP00000498155.1:p.Ala1258Val
|
|
ENST00000346085.9:c.3773C>T
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ENSP00000344546.4:p.Ala1258Val
|
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ENST00000350026.9:c.3734C>T
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ENSP00000055163.7:p.Ala1245Val
|
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ENST00000414678.6:c.2300C>T
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ENSP00000412835.2:p.Ala767Val
|
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NM_017519.2:c.3734C>T
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NP_059989.2:p.Ala1245Val
|
|
NM_020732.3:c.3773C>T
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NP_065783.3:p.Ala1258Val
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XM_005267069.3:c.3893C>T
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XP_005267126.2:p.Ala1298Val
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XM_011535984.1:c.2972C>T
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XP_011534286.1:p.Ala991Val
|
|
XM_011535985.1:c.2792C>T
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XP_011534287.1:p.Ala931Val
|
|
XM_011535986.1:c.2552C>T
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XP_011534288.1:p.Ala851Val
|
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XM_011535987.1:c.2171C>T
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XP_011534289.1:p.Ala724Val
|
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XM_011535988.1:c.1034C>T
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XP_011534290.1:p.Ala345Val
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NM_001346813.1:c.3893C>T
|
NP_001333742.1:p.Ala1298Val
|
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NM_001363725.1:c.1643C>T
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NP_001350654.1:p.Ala548Val
|
|
XM_011535984.2:c.4103C>T
|
XP_011534286.2:p.Ala1368Val
|
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XM_011535988.3:c.1034C>T
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XP_011534290.1:p.Ala345Val
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XM_017011103.2:c.4004C>T
|
XP_016866592.1:p.Ala1335Val
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XM_017011104.1:c.3974C>T
|
XP_016866593.1:p.Ala1325Val
|
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XM_017011105.2:c.3944C>T
|
XP_016866594.1:p.Ala1315Val
|
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XM_017011106.2:c.3815C>T
|
XP_016866595.1:p.Ala1272Val
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XM_017011107.2:c.3794C>T
|
XP_016866596.1:p.Ala1265Val
|
|
XR_002956289.1:n.4186C>T
|
|
|
NM_001363725.2:c.1643C>T
|
NP_001350654.1:p.Ala548Val
|
|
NM_001371656.1:c.4022C>T
|
NP_001358585.1:p.Ala1341Val
|
|
NM_001374820.1:c.4022C>T
|
NP_001361749.1:p.Ala1341Val
|
|
NM_001374828.1:c.4142C>T
MANE Select
|
NP_001361757.1:p.Ala1381Val
|
|
NM_017519.3:c.3983C>T
|
NP_059989.3:p.Ala1328Val
|
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