ENST00000695651.1:n.903A>G
|
|
|
ENST00000695652.1:c.2432A>G
|
ENSP00000512083.1:p.Tyr811Cys
|
|
ENST00000695653.1:c.464A>G
|
ENSP00000512084.1:p.Tyr155Cys
|
|
ENST00000695654.1:c.1679A>G
|
ENSP00000512085.1:p.Tyr560Cys
|
|
ENST00000695655.1:c.1496A>G
|
ENSP00000512086.1:n.1496A>G
|
|
ENST00000695692.1:n.1919A>G
|
|
|
ENST00000245907.11:c.2555A>G
MANE Select
|
ENSP00000245907.4:p.Tyr852Cys
|
|
ENST00000245907.10:c.2555A>G
|
ENSP00000245907.4:p.Tyr852Cys
|
|
ENST00000594005.1:n.36A>G
|
|
|
ENST00000602053.1:n.603A>G
|
|
|
NM_000064.3:c.2555A>G
|
NP_000055.2:p.Tyr852Cys
|
|
NM_000064.4:c.2555A>G
MANE Select
|
NP_000055.2:p.Tyr852Cys
|
|