|
ENST00000350026.11:c.4398C>G
|
ENSP00000055163.8:p.Tyr1466Ter
|
|
|
ENST00000414678.8:c.4467C>G
|
ENSP00000412835.3:p.Tyr1489Ter
|
|
|
ENST00000637015.2:c.4686C>G
|
ENSP00000489729.2:p.Tyr1562Ter
|
|
|
ENST00000346085.10:c.4437C>G
|
ENSP00000344546.5:p.Tyr1479Ter
|
|
|
ENST00000350026.10:c.4149C>G
|
ENSP00000055163.7:p.Tyr1383Ter
|
|
|
ENST00000414678.7:c.2715C>G
|
ENSP00000412835.2:p.Tyr905Ter
|
|
|
ENST00000635849.1:c.1878C>G
|
ENSP00000490948.1:p.Tyr626Ter
|
|
|
ENST00000635957.1:c.1509C>G
|
ENSP00000490385.1:p.Tyr503Ter
|
|
|
ENST00000636227.1:n.3020C>G
|
|
|
|
ENST00000636254.1:n.477C>G
|
|
|
|
ENST00000636930.2:c.4557C>G
MANE Select
|
ENSP00000490491.2:p.Tyr1519Ter
|
|
|
ENST00000636940.1:n.2554C>G
|
|
|
|
ENST00000637015.1:c.1925C>G
|
|
|
|
ENST00000637568.1:c.1839C>G
|
|
|
|
ENST00000637741.1:n.1223C>G
|
|
|
|
ENST00000637810.1:c.1899C>G
|
ENSP00000489636.1:p.Tyr633Ter
|
|
|
ENST00000637904.1:c.2058C>G
|
ENSP00000490550.1:p.Tyr686Ter
|
|
|
ENST00000647938.1:c.4188C>G
|
ENSP00000498155.1:p.Tyr1396Ter
|
|
|
ENST00000346085.9:c.4188C>G
|
ENSP00000344546.4:p.Tyr1396Ter
|
|
|
ENST00000350026.9:c.4149C>G
|
ENSP00000055163.7:p.Tyr1383Ter
|
|
|
ENST00000414678.6:c.2715C>G
|
ENSP00000412835.2:p.Tyr905Ter
|
|
|
NM_017519.2:c.4149C>G
|
NP_059989.2:p.Tyr1383Ter
|
|
|
NM_020732.3:c.4188C>G
|
NP_065783.3:p.Tyr1396Ter
|
|
|
XM_005267069.3:c.4308C>G
|
XP_005267126.2:p.Tyr1436Ter
|
|
|
XM_011535984.1:c.3387C>G
|
XP_011534286.1:p.Tyr1129Ter
|
|
|
XM_011535985.1:c.3207C>G
|
XP_011534287.1:p.Tyr1069Ter
|
|
|
XM_011535986.1:c.2967C>G
|
XP_011534288.1:p.Tyr989Ter
|
|
|
XM_011535987.1:c.2586C>G
|
XP_011534289.1:p.Tyr862Ter
|
|
|
XM_011535988.1:c.1449C>G
|
XP_011534290.1:p.Tyr483Ter
|
|
|
NM_001346813.1:c.4308C>G
|
NP_001333742.1:p.Tyr1436Ter
|
|
|
NM_001363725.1:c.2058C>G
|
NP_001350654.1:p.Tyr686Ter
|
|
|
XM_011535984.2:c.4518C>G
|
XP_011534286.2:p.Tyr1506Ter
|
|
|
XM_011535988.3:c.1449C>G
|
XP_011534290.1:p.Tyr483Ter
|
|
|
XM_017011103.2:c.4419C>G
|
XP_016866592.1:p.Tyr1473Ter
|
|
|
XM_017011104.1:c.4389C>G
|
XP_016866593.1:p.Tyr1463Ter
|
|
|
XM_017011105.2:c.4359C>G
|
XP_016866594.1:p.Tyr1453Ter
|
|
|
XM_017011106.2:c.4230C>G
|
XP_016866595.1:p.Tyr1410Ter
|
|
|
XM_017011107.2:c.4209C>G
|
XP_016866596.1:p.Tyr1403Ter
|
|
|
XR_002956289.1:n.4504C>G
|
|
|
|
NM_001363725.2:c.2058C>G
|
NP_001350654.1:p.Tyr686Ter
|
|
|
NM_001371656.1:c.4437C>G
|
NP_001358585.1:p.Tyr1479Ter
|
|
|
NM_001374820.1:c.4437C>G
|
NP_001361749.1:p.Tyr1479Ter
|
|
|
NM_001374828.1:c.4557C>G
MANE Select
|
NP_001361757.1:p.Tyr1519Ter
|
|
|
NM_017519.3:c.4398C>G
|
NP_059989.3:p.Tyr1466Ter
|
|
