ENST00000350026.11:c.4862C>G
|
ENSP00000055163.8:p.Ser1621Cys
|
|
ENST00000414678.8:c.4931C>G
|
ENSP00000412835.3:p.Ser1644Cys
|
|
ENST00000637015.2:c.5150C>G
|
ENSP00000489729.2:p.Ser1717Cys
|
|
ENST00000346085.10:c.4901C>G
|
ENSP00000344546.5:p.Ser1634Cys
|
|
ENST00000350026.10:c.4613C>G
|
ENSP00000055163.7:p.Ser1538Cys
|
|
ENST00000414678.7:c.3179C>G
|
ENSP00000412835.2:p.Ser1060Cys
|
|
ENST00000635849.1:c.2342C>G
|
ENSP00000490948.1:p.Ser781Cys
|
|
ENST00000635957.1:c.1973C>G
|
ENSP00000490385.1:p.Ser658Cys
|
|
ENST00000636227.1:n.3484C>G
|
|
|
ENST00000636254.1:n.941C>G
|
|
|
ENST00000636930.2:c.5021C>G
MANE Select
|
ENSP00000490491.2:p.Ser1674Cys
|
|
ENST00000636940.1:n.3018C>G
|
|
|
ENST00000637015.1:c.2389C>G
|
|
|
ENST00000637568.1:c.2303C>G
|
|
|
ENST00000637741.1:n.1687C>G
|
|
|
ENST00000637810.1:c.2363C>G
|
ENSP00000489636.1:p.Ser788Cys
|
|
ENST00000637904.1:c.2522C>G
|
ENSP00000490550.1:p.Ser841Cys
|
|
ENST00000647938.1:c.4652C>G
|
ENSP00000498155.1:p.Ser1551Cys
|
|
ENST00000346085.9:c.4652C>G
|
ENSP00000344546.4:p.Ser1551Cys
|
|
ENST00000350026.9:c.4613C>G
|
ENSP00000055163.7:p.Ser1538Cys
|
|
ENST00000414678.6:c.3179C>G
|
ENSP00000412835.2:p.Ser1060Cys
|
|
NM_017519.2:c.4613C>G
|
NP_059989.2:p.Ser1538Cys
|
|
NM_020732.3:c.4652C>G
|
NP_065783.3:p.Ser1551Cys
|
|
XM_005267069.3:c.4772C>G
|
XP_005267126.2:p.Ser1591Cys
|
|
XM_011535984.1:c.3851C>G
|
XP_011534286.1:p.Ser1284Cys
|
|
XM_011535985.1:c.3671C>G
|
XP_011534287.1:p.Ser1224Cys
|
|
XM_011535986.1:c.3431C>G
|
XP_011534288.1:p.Ser1144Cys
|
|
XM_011535987.1:c.3050C>G
|
XP_011534289.1:p.Ser1017Cys
|
|
XM_011535988.1:c.1913C>G
|
XP_011534290.1:p.Ser638Cys
|
|
NM_001346813.1:c.4772C>G
|
NP_001333742.1:p.Ser1591Cys
|
|
NM_001363725.1:c.2522C>G
|
NP_001350654.1:p.Ser841Cys
|
|
XM_011535984.2:c.4982C>G
|
XP_011534286.2:p.Ser1661Cys
|
|
XM_011535988.3:c.1913C>G
|
XP_011534290.1:p.Ser638Cys
|
|
XM_017011103.2:c.4883C>G
|
XP_016866592.1:p.Ser1628Cys
|
|
XM_017011104.1:c.4853C>G
|
XP_016866593.1:p.Ser1618Cys
|
|
XM_017011105.2:c.4823C>G
|
XP_016866594.1:p.Ser1608Cys
|
|
XM_017011106.2:c.4694C>G
|
XP_016866595.1:p.Ser1565Cys
|
|
XM_017011107.2:c.4673C>G
|
XP_016866596.1:p.Ser1558Cys
|
|
XR_002956289.1:n.4968C>G
|
|
|
NM_001363725.2:c.2522C>G
|
NP_001350654.1:p.Ser841Cys
|
|
NM_001371656.1:c.4901C>G
|
NP_001358585.1:p.Ser1634Cys
|
|
NM_001374820.1:c.4901C>G
|
NP_001361749.1:p.Ser1634Cys
|
|
NM_001374828.1:c.5021C>G
MANE Select
|
NP_001361757.1:p.Ser1674Cys
|
|
NM_017519.3:c.4862C>G
|
NP_059989.3:p.Ser1621Cys
|
|