ENST00000695651.1:n.966G>A
|
|
|
ENST00000695652.1:c.2495G>A
|
ENSP00000512083.1:p.Cys832Tyr
|
|
ENST00000695653.1:c.527G>A
|
ENSP00000512084.1:p.Cys176Tyr
|
|
ENST00000695654.1:c.1742G>A
|
ENSP00000512085.1:p.Cys581Tyr
|
|
ENST00000695655.1:c.1559G>A
|
ENSP00000512086.1:n.1559G>A
|
|
ENST00000695692.1:n.1982G>A
|
|
|
ENST00000245907.11:c.2618G>A
MANE Select
|
ENSP00000245907.4:p.Cys873Tyr
|
|
ENST00000245907.10:c.2618G>A
|
ENSP00000245907.4:p.Cys873Tyr
|
|
ENST00000594005.1:n.194G>A
|
|
|
NM_000064.3:c.2618G>A
|
NP_000055.2:p.Cys873Tyr
|
|
NM_000064.4:c.2618G>A
MANE Select
|
NP_000055.2:p.Cys873Tyr
|
|