ENST00000274576.9:c.918del
MANE Select
|
ENSP00000274576.5:p.Tyr307MetfsTer2
|
|
ENST00000274576.8:c.918del
|
ENSP00000274576.4:p.Tyr307MetfsTer2
|
|
ENST00000455880.2:c.918del
|
ENSP00000411593.2:p.Tyr307MetfsTer2
|
|
ENST00000462581.6:c.*676del
|
ENSP00000430595.1:n.*676del
|
|
NM_000171.3:c.918del
|
NP_000162.2:p.Tyr307MetfsTer2
|
|
NM_001146040.1:c.918del
|
NP_001139512.1:p.Tyr307MetfsTer2
|
|
NM_001292000.1:c.669del
|
NP_001278929.1:p.Tyr224MetfsTer2
|
|
NM_000171.4:c.918del
MANE Select
|
NP_000162.2:p.Tyr307MetfsTer2
|
|
NM_001146040.2:c.918del
|
NP_001139512.1:p.Tyr307MetfsTer2
|
|
NM_001292000.2:c.669del
|
NP_001278929.1:p.Tyr224MetfsTer2
|
|