ENST00000695651.1:n.1098A>G
|
|
|
ENST00000695652.1:c.2627A>G
|
ENSP00000512083.1:p.Tyr876Cys
|
|
ENST00000695653.1:c.659A>G
|
ENSP00000512084.1:p.Tyr220Cys
|
|
ENST00000695654.1:c.1874A>G
|
ENSP00000512085.1:p.Tyr625Cys
|
|
ENST00000695655.1:c.1691A>G
|
ENSP00000512086.1:n.1691A>G
|
|
ENST00000695692.1:n.2114A>G
|
|
|
ENST00000245907.11:c.2750A>G
MANE Select
|
ENSP00000245907.4:p.Tyr917Cys
|
|
ENST00000245907.10:c.2750A>G
|
ENSP00000245907.4:p.Tyr917Cys
|
|
ENST00000594005.1:n.326A>G
|
|
|
NM_000064.3:c.2750A>G
|
NP_000055.2:p.Tyr917Cys
|
|
NM_000064.4:c.2750A>G
MANE Select
|
NP_000055.2:p.Tyr917Cys
|
|