ENST00000274576.9:c.836C>T
MANE Select
|
ENSP00000274576.5:p.Ala279Val
|
|
ENST00000274576.8:c.836C>T
|
ENSP00000274576.4:p.Ala279Val
|
|
ENST00000455880.2:c.836C>T
|
ENSP00000411593.2:p.Ala279Val
|
|
ENST00000462581.6:c.*594C>T
|
ENSP00000430595.1:n.*594C>T
|
|
ENST00000471351.2:n.1119C>T
|
|
|
NM_000171.3:c.836C>T
|
NP_000162.2:p.Ala279Val
|
|
NM_001146040.1:c.836C>T
|
NP_001139512.1:p.Ala279Val
|
|
NM_001292000.1:c.587C>T
|
NP_001278929.1:p.Ala196Val
|
|
XM_005268412.2:c.836C>T
|
XP_005268469.1:p.Ala279Val
|
|
NM_000171.4:c.836C>T
MANE Select
|
NP_000162.2:p.Ala279Val
|
|
NM_001146040.2:c.836C>T
|
NP_001139512.1:p.Ala279Val
|
|
NM_001292000.2:c.587C>T
|
NP_001278929.1:p.Ala196Val
|
|