ENST00000274576.9:c.968T>A
MANE Select
|
ENSP00000274576.5:p.Phe323Tyr
|
|
ENST00000274576.8:c.968T>A
|
ENSP00000274576.4:p.Phe323Tyr
|
|
ENST00000455880.2:c.968T>A
|
ENSP00000411593.2:p.Phe323Tyr
|
|
ENST00000462581.6:c.*726T>A
|
ENSP00000430595.1:n.*726T>A
|
|
NM_000171.3:c.968T>A
|
NP_000162.2:p.Phe323Tyr
|
|
NM_001146040.1:c.968T>A
|
NP_001139512.1:p.Phe323Tyr
|
|
NM_001292000.1:c.719T>A
|
NP_001278929.1:p.Phe240Tyr
|
|
NM_000171.4:c.968T>A
MANE Select
|
NP_000162.2:p.Phe323Tyr
|
|
NM_001146040.2:c.968T>A
|
NP_001139512.1:p.Phe323Tyr
|
|
NM_001292000.2:c.719T>A
|
NP_001278929.1:p.Phe240Tyr
|
|