ENST00000312465.12:c.782A>G
MANE Select
|
ENSP00000311697.7:p.Tyr261Cys
|
|
ENST00000312465.11:c.782A>G
|
ENSP00000311697.7:p.Tyr261Cys
|
|
ENST00000456523.3:c.*306A>G
|
ENSP00000398353.3:n.*306A>G
|
|
ENST00000503413.1:n.731A>G
|
|
|
ENST00000507780.1:c.342+11635A>G
|
ENSP00000423903.1:n.342+11635A>G
|
|
NM_001291812.1:c.353A>G
|
NP_001278741.1:p.Tyr118Cys
|
|
NM_004464.3:c.782A>G
|
NP_004455.2:p.Tyr261Cys
|
|
NM_033143.2:c.*306A>G
|
NP_149134.1:n.*306A>G
|
|
NM_001291812.2:c.353A>G
|
NP_001278741.1:p.Tyr118Cys
|
|
NM_004464.4:c.782A>G
MANE Select
|
NP_004455.2:p.Tyr261Cys
|
|