ENST00000350026.11:c.3950C>A
|
ENSP00000055163.8:p.Ser1317Tyr
|
|
ENST00000414678.8:c.4019C>A
|
ENSP00000412835.3:p.Ser1340Tyr
|
|
ENST00000637015.2:c.4238C>A
|
ENSP00000489729.2:p.Ser1413Tyr
|
|
ENST00000346085.10:c.3989C>A
|
ENSP00000344546.5:p.Ser1330Tyr
|
|
ENST00000350026.10:c.3701C>A
|
ENSP00000055163.7:p.Ser1234Tyr
|
|
ENST00000414678.7:c.2267C>A
|
ENSP00000412835.2:p.Ser756Tyr
|
|
ENST00000635849.1:c.1430C>A
|
ENSP00000490948.1:p.Ser477Tyr
|
|
ENST00000635957.1:c.1061C>A
|
ENSP00000490385.1:p.Ser354Tyr
|
|
ENST00000636930.2:c.4109C>A
MANE Select
|
ENSP00000490491.2:p.Ser1370Tyr
|
|
ENST00000636940.1:n.2106C>A
|
|
|
ENST00000637015.1:c.1477C>A
|
|
|
ENST00000637568.1:c.1391C>A
|
|
|
ENST00000637741.1:n.775C>A
|
|
|
ENST00000637810.1:c.1451C>A
|
ENSP00000489636.1:p.Ser484Tyr
|
|
ENST00000637904.1:c.1610C>A
|
ENSP00000490550.1:p.Ser537Tyr
|
|
ENST00000647938.1:c.3740C>A
|
ENSP00000498155.1:p.Ser1247Tyr
|
|
ENST00000346085.9:c.3740C>A
|
ENSP00000344546.4:p.Ser1247Tyr
|
|
ENST00000350026.9:c.3701C>A
|
ENSP00000055163.7:p.Ser1234Tyr
|
|
ENST00000414678.6:c.2267C>A
|
ENSP00000412835.2:p.Ser756Tyr
|
|
NM_017519.2:c.3701C>A
|
NP_059989.2:p.Ser1234Tyr
|
|
NM_020732.3:c.3740C>A
|
NP_065783.3:p.Ser1247Tyr
|
|
XM_005267069.3:c.3860C>A
|
XP_005267126.2:p.Ser1287Tyr
|
|
XM_011535984.1:c.2939C>A
|
XP_011534286.1:p.Ser980Tyr
|
|
XM_011535985.1:c.2759C>A
|
XP_011534287.1:p.Ser920Tyr
|
|
XM_011535986.1:c.2519C>A
|
XP_011534288.1:p.Ser840Tyr
|
|
XM_011535987.1:c.2138C>A
|
XP_011534289.1:p.Ser713Tyr
|
|
XM_011535988.1:c.1001C>A
|
XP_011534290.1:p.Ser334Tyr
|
|
NM_001346813.1:c.3860C>A
|
NP_001333742.1:p.Ser1287Tyr
|
|
NM_001363725.1:c.1610C>A
|
NP_001350654.1:p.Ser537Tyr
|
|
XM_011535984.2:c.4070C>A
|
XP_011534286.2:p.Ser1357Tyr
|
|
XM_011535988.3:c.1001C>A
|
XP_011534290.1:p.Ser334Tyr
|
|
XM_017011103.2:c.3971C>A
|
XP_016866592.1:p.Ser1324Tyr
|
|
XM_017011104.1:c.3941C>A
|
XP_016866593.1:p.Ser1314Tyr
|
|
XM_017011105.2:c.3911C>A
|
XP_016866594.1:p.Ser1304Tyr
|
|
XM_017011106.2:c.3782C>A
|
XP_016866595.1:p.Ser1261Tyr
|
|
XM_017011107.2:c.3761C>A
|
XP_016866596.1:p.Ser1254Tyr
|
|
XR_002956289.1:n.4153C>A
|
|
|
NM_001363725.2:c.1610C>A
|
NP_001350654.1:p.Ser537Tyr
|
|
NM_001371656.1:c.3989C>A
|
NP_001358585.1:p.Ser1330Tyr
|
|
NM_001374820.1:c.3989C>A
|
NP_001361749.1:p.Ser1330Tyr
|
|
NM_001374828.1:c.4109C>A
MANE Select
|
NP_001361757.1:p.Ser1370Tyr
|
|
NM_017519.3:c.3950C>A
|
NP_059989.3:p.Ser1317Tyr
|
|