ENST00000312465.12:c.598C>T
MANE Select
|
ENSP00000311697.7:p.Arg200Ter
|
|
ENST00000312465.11:c.598C>T
|
ENSP00000311697.7:p.Arg200Ter
|
|
ENST00000456523.3:c.*122C>T
|
ENSP00000398353.3:n.*122C>T
|
|
ENST00000503413.1:n.547C>T
|
|
|
ENST00000507780.1:c.342+11451C>T
|
ENSP00000423903.1:n.342+11451C>T
|
|
NM_001291812.1:c.169C>T
|
NP_001278741.1:p.Arg57Ter
|
|
NM_004464.3:c.598C>T
|
NP_004455.2:p.Arg200Ter
|
|
NM_033143.2:c.*122C>T
|
NP_149134.1:n.*122C>T
|
|
NM_001291812.2:c.169C>T
|
NP_001278741.1:p.Arg57Ter
|
|
NM_004464.4:c.598C>T
MANE Select
|
NP_004455.2:p.Arg200Ter
|
|