ENST00000350026.11:c.3983C>G
|
ENSP00000055163.8:p.Ala1328Gly
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ENST00000414678.8:c.4052C>G
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ENSP00000412835.3:p.Ala1351Gly
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ENST00000637015.2:c.4271C>G
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ENSP00000489729.2:p.Ala1424Gly
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ENST00000346085.10:c.4022C>G
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ENSP00000344546.5:p.Ala1341Gly
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ENST00000350026.10:c.3734C>G
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ENSP00000055163.7:p.Ala1245Gly
|
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ENST00000414678.7:c.2300C>G
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ENSP00000412835.2:p.Ala767Gly
|
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ENST00000635849.1:c.1463C>G
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ENSP00000490948.1:p.Ala488Gly
|
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ENST00000635957.1:c.1094C>G
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ENSP00000490385.1:p.Ala365Gly
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ENST00000636930.2:c.4142C>G
MANE Select
|
ENSP00000490491.2:p.Ala1381Gly
|
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ENST00000636940.1:n.2139C>G
|
|
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ENST00000637015.1:c.1510C>G
|
|
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ENST00000637568.1:c.1424C>G
|
|
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ENST00000637741.1:n.808C>G
|
|
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ENST00000637810.1:c.1484C>G
|
ENSP00000489636.1:p.Ala495Gly
|
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ENST00000637904.1:c.1643C>G
|
ENSP00000490550.1:p.Ala548Gly
|
|
ENST00000647938.1:c.3773C>G
|
ENSP00000498155.1:p.Ala1258Gly
|
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ENST00000346085.9:c.3773C>G
|
ENSP00000344546.4:p.Ala1258Gly
|
|
ENST00000350026.9:c.3734C>G
|
ENSP00000055163.7:p.Ala1245Gly
|
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ENST00000414678.6:c.2300C>G
|
ENSP00000412835.2:p.Ala767Gly
|
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NM_017519.2:c.3734C>G
|
NP_059989.2:p.Ala1245Gly
|
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NM_020732.3:c.3773C>G
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NP_065783.3:p.Ala1258Gly
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XM_005267069.3:c.3893C>G
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XP_005267126.2:p.Ala1298Gly
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XM_011535984.1:c.2972C>G
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XP_011534286.1:p.Ala991Gly
|
|
XM_011535985.1:c.2792C>G
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XP_011534287.1:p.Ala931Gly
|
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XM_011535986.1:c.2552C>G
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XP_011534288.1:p.Ala851Gly
|
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XM_011535987.1:c.2171C>G
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XP_011534289.1:p.Ala724Gly
|
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XM_011535988.1:c.1034C>G
|
XP_011534290.1:p.Ala345Gly
|
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NM_001346813.1:c.3893C>G
|
NP_001333742.1:p.Ala1298Gly
|
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NM_001363725.1:c.1643C>G
|
NP_001350654.1:p.Ala548Gly
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XM_011535984.2:c.4103C>G
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XP_011534286.2:p.Ala1368Gly
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XM_011535988.3:c.1034C>G
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XP_011534290.1:p.Ala345Gly
|
|
XM_017011103.2:c.4004C>G
|
XP_016866592.1:p.Ala1335Gly
|
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XM_017011104.1:c.3974C>G
|
XP_016866593.1:p.Ala1325Gly
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XM_017011105.2:c.3944C>G
|
XP_016866594.1:p.Ala1315Gly
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XM_017011106.2:c.3815C>G
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XP_016866595.1:p.Ala1272Gly
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XM_017011107.2:c.3794C>G
|
XP_016866596.1:p.Ala1265Gly
|
|
XR_002956289.1:n.4186C>G
|
|
|
NM_001363725.2:c.1643C>G
|
NP_001350654.1:p.Ala548Gly
|
|
NM_001371656.1:c.4022C>G
|
NP_001358585.1:p.Ala1341Gly
|
|
NM_001374820.1:c.4022C>G
|
NP_001361749.1:p.Ala1341Gly
|
|
NM_001374828.1:c.4142C>G
MANE Select
|
NP_001361757.1:p.Ala1381Gly
|
|
NM_017519.3:c.3983C>G
|
NP_059989.3:p.Ala1328Gly
|
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