ENST00000563588.6:c.416A>T
MANE Select
|
ENSP00000455607.1:p.Glu139Val
|
|
ENST00000328273.11:c.416A>T
|
ENSP00000329968.7:p.Glu139Val
|
|
ENST00000424889.7:c.416A>T
|
ENSP00000388571.3:p.Glu139Val
|
|
ENST00000561712.1:c.90A>T
|
|
|
ENST00000563588.5:c.416A>T
|
ENSP00000455607.1:p.Glu139Val
|
|
ENST00000563607.1:c.*88A>T
|
ENSP00000454641.1:n.*88A>T
|
|
ENST00000563913.5:n.749A>T
|
|
|
ENST00000564838.5:n.790A>T
|
|
|
ENST00000565897.5:c.416A>T
|
ENSP00000457359.1:p.Glu139Val
|
|
ENST00000565924.5:c.416A>T
|
ENSP00000455091.1:p.Glu139Val
|
|
ENST00000569684.1:n.828A>T
|
|
|
NM_000294.2:c.416A>T
|
NP_000285.1:p.Glu139Val
|
|
NM_001172432.1:c.416A>T
|
NP_001165903.1:p.Glu139Val
|
|
NM_000294.3:c.416A>T
MANE Select
|
NP_000285.1:p.Glu139Val
|
|
NM_001172432.2:c.416A>T
|
NP_001165903.1:p.Glu139Val
|
|