ENST00000350026.11:c.3950C>G
|
ENSP00000055163.8:p.Ser1317Cys
|
|
ENST00000414678.8:c.4019C>G
|
ENSP00000412835.3:p.Ser1340Cys
|
|
ENST00000637015.2:c.4238C>G
|
ENSP00000489729.2:p.Ser1413Cys
|
|
ENST00000346085.10:c.3989C>G
|
ENSP00000344546.5:p.Ser1330Cys
|
|
ENST00000350026.10:c.3701C>G
|
ENSP00000055163.7:p.Ser1234Cys
|
|
ENST00000414678.7:c.2267C>G
|
ENSP00000412835.2:p.Ser756Cys
|
|
ENST00000635849.1:c.1430C>G
|
ENSP00000490948.1:p.Ser477Cys
|
|
ENST00000635957.1:c.1061C>G
|
ENSP00000490385.1:p.Ser354Cys
|
|
ENST00000636930.2:c.4109C>G
MANE Select
|
ENSP00000490491.2:p.Ser1370Cys
|
|
ENST00000636940.1:n.2106C>G
|
|
|
ENST00000637015.1:c.1477C>G
|
|
|
ENST00000637568.1:c.1391C>G
|
|
|
ENST00000637741.1:n.775C>G
|
|
|
ENST00000637810.1:c.1451C>G
|
ENSP00000489636.1:p.Ser484Cys
|
|
ENST00000637904.1:c.1610C>G
|
ENSP00000490550.1:p.Ser537Cys
|
|
ENST00000647938.1:c.3740C>G
|
ENSP00000498155.1:p.Ser1247Cys
|
|
ENST00000346085.9:c.3740C>G
|
ENSP00000344546.4:p.Ser1247Cys
|
|
ENST00000350026.9:c.3701C>G
|
ENSP00000055163.7:p.Ser1234Cys
|
|
ENST00000414678.6:c.2267C>G
|
ENSP00000412835.2:p.Ser756Cys
|
|
NM_017519.2:c.3701C>G
|
NP_059989.2:p.Ser1234Cys
|
|
NM_020732.3:c.3740C>G
|
NP_065783.3:p.Ser1247Cys
|
|
XM_005267069.3:c.3860C>G
|
XP_005267126.2:p.Ser1287Cys
|
|
XM_011535984.1:c.2939C>G
|
XP_011534286.1:p.Ser980Cys
|
|
XM_011535985.1:c.2759C>G
|
XP_011534287.1:p.Ser920Cys
|
|
XM_011535986.1:c.2519C>G
|
XP_011534288.1:p.Ser840Cys
|
|
XM_011535987.1:c.2138C>G
|
XP_011534289.1:p.Ser713Cys
|
|
XM_011535988.1:c.1001C>G
|
XP_011534290.1:p.Ser334Cys
|
|
NM_001346813.1:c.3860C>G
|
NP_001333742.1:p.Ser1287Cys
|
|
NM_001363725.1:c.1610C>G
|
NP_001350654.1:p.Ser537Cys
|
|
XM_011535984.2:c.4070C>G
|
XP_011534286.2:p.Ser1357Cys
|
|
XM_011535988.3:c.1001C>G
|
XP_011534290.1:p.Ser334Cys
|
|
XM_017011103.2:c.3971C>G
|
XP_016866592.1:p.Ser1324Cys
|
|
XM_017011104.1:c.3941C>G
|
XP_016866593.1:p.Ser1314Cys
|
|
XM_017011105.2:c.3911C>G
|
XP_016866594.1:p.Ser1304Cys
|
|
XM_017011106.2:c.3782C>G
|
XP_016866595.1:p.Ser1261Cys
|
|
XM_017011107.2:c.3761C>G
|
XP_016866596.1:p.Ser1254Cys
|
|
XR_002956289.1:n.4153C>G
|
|
|
NM_001363725.2:c.1610C>G
|
NP_001350654.1:p.Ser537Cys
|
|
NM_001371656.1:c.3989C>G
|
NP_001358585.1:p.Ser1330Cys
|
|
NM_001374820.1:c.3989C>G
|
NP_001361749.1:p.Ser1330Cys
|
|
NM_001374828.1:c.4109C>G
MANE Select
|
NP_001361757.1:p.Ser1370Cys
|
|
NM_017519.3:c.3950C>G
|
NP_059989.3:p.Ser1317Cys
|
|