ENST00000695651.1:n.2145A>G
|
|
|
ENST00000695652.1:c.3674A>G
|
ENSP00000512083.1:p.Tyr1225Cys
|
|
ENST00000695653.1:c.1706A>G
|
ENSP00000512084.1:p.Tyr569Cys
|
|
ENST00000695654.1:c.2822A>G
|
ENSP00000512085.1:p.Tyr941Cys
|
|
ENST00000695655.1:c.2738A>G
|
ENSP00000512086.1:n.2738A>G
|
|
ENST00000695692.1:n.3161A>G
|
|
|
ENST00000245907.11:c.3797A>G
MANE Select
|
ENSP00000245907.4:p.Tyr1266Cys
|
|
ENST00000245907.10:c.3797A>G
|
ENSP00000245907.4:p.Tyr1266Cys
|
|
ENST00000596238.1:n.240A>G
|
|
|
ENST00000601008.1:c.241+609A>G
|
ENSP00000471384.1:n.241+609A>G
|
|
NM_000064.3:c.3797A>G
|
NP_000055.2:p.Tyr1266Cys
|
|
NM_000064.4:c.3797A>G
MANE Select
|
NP_000055.2:p.Tyr1266Cys
|
|