ENST00000350026.11:c.4680C>A
|
ENSP00000055163.8:p.Tyr1560Ter
|
|
ENST00000414678.8:c.4749C>A
|
ENSP00000412835.3:p.Tyr1583Ter
|
|
ENST00000637015.2:c.4968C>A
|
ENSP00000489729.2:p.Tyr1656Ter
|
|
ENST00000346085.10:c.4719C>A
|
ENSP00000344546.5:p.Tyr1573Ter
|
|
ENST00000350026.10:c.4431C>A
|
ENSP00000055163.7:p.Tyr1477Ter
|
|
ENST00000414678.7:c.2997C>A
|
ENSP00000412835.2:p.Tyr999Ter
|
|
ENST00000635849.1:c.2160C>A
|
ENSP00000490948.1:p.Tyr720Ter
|
|
ENST00000635957.1:c.1791C>A
|
ENSP00000490385.1:p.Tyr597Ter
|
|
ENST00000636227.1:n.3302C>A
|
|
|
ENST00000636254.1:n.759C>A
|
|
|
ENST00000636930.2:c.4839C>A
MANE Select
|
ENSP00000490491.2:p.Tyr1613Ter
|
|
ENST00000636940.1:n.2836C>A
|
|
|
ENST00000637015.1:c.2207C>A
|
|
|
ENST00000637568.1:c.2121C>A
|
|
|
ENST00000637741.1:n.1505C>A
|
|
|
ENST00000637810.1:c.2181C>A
|
ENSP00000489636.1:p.Tyr727Ter
|
|
ENST00000637904.1:c.2340C>A
|
ENSP00000490550.1:p.Tyr780Ter
|
|
ENST00000647938.1:c.4470C>A
|
ENSP00000498155.1:p.Tyr1490Ter
|
|
ENST00000346085.9:c.4470C>A
|
ENSP00000344546.4:p.Tyr1490Ter
|
|
ENST00000350026.9:c.4431C>A
|
ENSP00000055163.7:p.Tyr1477Ter
|
|
ENST00000414678.6:c.2997C>A
|
ENSP00000412835.2:p.Tyr999Ter
|
|
NM_017519.2:c.4431C>A
|
NP_059989.2:p.Tyr1477Ter
|
|
NM_020732.3:c.4470C>A
|
NP_065783.3:p.Tyr1490Ter
|
|
XM_005267069.3:c.4590C>A
|
XP_005267126.2:p.Tyr1530Ter
|
|
XM_011535984.1:c.3669C>A
|
XP_011534286.1:p.Tyr1223Ter
|
|
XM_011535985.1:c.3489C>A
|
XP_011534287.1:p.Tyr1163Ter
|
|
XM_011535986.1:c.3249C>A
|
XP_011534288.1:p.Tyr1083Ter
|
|
XM_011535987.1:c.2868C>A
|
XP_011534289.1:p.Tyr956Ter
|
|
XM_011535988.1:c.1731C>A
|
XP_011534290.1:p.Tyr577Ter
|
|
NM_001346813.1:c.4590C>A
|
NP_001333742.1:p.Tyr1530Ter
|
|
NM_001363725.1:c.2340C>A
|
NP_001350654.1:p.Tyr780Ter
|
|
XM_011535984.2:c.4800C>A
|
XP_011534286.2:p.Tyr1600Ter
|
|
XM_011535988.3:c.1731C>A
|
XP_011534290.1:p.Tyr577Ter
|
|
XM_017011103.2:c.4701C>A
|
XP_016866592.1:p.Tyr1567Ter
|
|
XM_017011104.1:c.4671C>A
|
XP_016866593.1:p.Tyr1557Ter
|
|
XM_017011105.2:c.4641C>A
|
XP_016866594.1:p.Tyr1547Ter
|
|
XM_017011106.2:c.4512C>A
|
XP_016866595.1:p.Tyr1504Ter
|
|
XM_017011107.2:c.4491C>A
|
XP_016866596.1:p.Tyr1497Ter
|
|
XR_002956289.1:n.4786C>A
|
|
|
NM_001363725.2:c.2340C>A
|
NP_001350654.1:p.Tyr780Ter
|
|
NM_001371656.1:c.4719C>A
|
NP_001358585.1:p.Tyr1573Ter
|
|
NM_001374820.1:c.4719C>A
|
NP_001361749.1:p.Tyr1573Ter
|
|
NM_001374828.1:c.4839C>A
MANE Select
|
NP_001361757.1:p.Tyr1613Ter
|
|
NM_017519.3:c.4680C>A
|
NP_059989.3:p.Tyr1560Ter
|
|