ENST00000398603.6:c.353A>G
|
ENSP00000381604.1:p.Tyr118Cys
|
|
ENST00000398606.10:c.461A>G
MANE Select
|
ENSP00000381607.3:p.Tyr154Cys
|
|
ENST00000646888.1:c.*177A>G
|
ENSP00000494477.1:n.*177A>G
|
|
ENST00000398603.5:c.353A>G
|
ENSP00000381604.1:p.Tyr118Cys
|
|
ENST00000398606.7:c.461A>G
|
ENSP00000381607.3:p.Tyr154Cys
|
|
ENST00000467591.1:n.572A>G
|
|
|
ENST00000494593.1:n.1433A>G
|
|
|
ENST00000495996.1:c.187A>G
|
ENSP00000484686.1:p.Thr63Ala
|
|
ENST00000498765.5:c.524A>G
|
|
|
NM_000852.3:c.461A>G , LRG_723t1:c.461A>G
|
NP_000843.1:p.Tyr154Cys
|
|
NM_000852.4:c.461A>G
MANE Select
|
NP_000843.1:p.Tyr154Cys
|
|