ENST00000695651.1:n.2085T>G
|
|
|
ENST00000695652.1:c.3614T>G
|
ENSP00000512083.1:p.Phe1205Cys
|
|
ENST00000695653.1:c.1646T>G
|
ENSP00000512084.1:p.Phe549Cys
|
|
ENST00000695654.1:c.2762T>G
|
ENSP00000512085.1:p.Phe921Cys
|
|
ENST00000695655.1:c.2678T>G
|
ENSP00000512086.1:n.2678T>G
|
|
ENST00000695692.1:n.3101T>G
|
|
|
ENST00000245907.11:c.3737T>G
MANE Select
|
ENSP00000245907.4:p.Phe1246Cys
|
|
ENST00000245907.10:c.3737T>G
|
ENSP00000245907.4:p.Phe1246Cys
|
|
ENST00000596238.1:n.180T>G
|
|
|
ENST00000601008.1:c.241+549T>G
|
ENSP00000471384.1:n.241+549T>G
|
|
NM_000064.3:c.3737T>G
|
NP_000055.2:p.Phe1246Cys
|
|
NM_000064.4:c.3737T>G
MANE Select
|
NP_000055.2:p.Phe1246Cys
|
|