ENST00000563588.6:c.522C>T
MANE Select
|
ENSP00000455607.1:p.Phe174=
|
|
ENST00000328273.11:c.522C>T
|
ENSP00000329968.7:p.Phe174=
|
|
ENST00000424889.7:c.522C>T
|
ENSP00000388571.3:p.Phe174=
|
|
ENST00000561712.1:c.196C>T
|
|
|
ENST00000563588.5:c.522C>T
|
ENSP00000455607.1:p.Phe174=
|
|
ENST00000563607.1:c.*194C>T
|
ENSP00000454641.1:n.*194C>T
|
|
ENST00000563913.5:n.855C>T
|
|
|
ENST00000564838.5:n.896C>T
|
|
|
ENST00000565897.5:c.522C>T
|
ENSP00000457359.1:p.Phe174=
|
|
ENST00000565924.5:c.522C>T
|
ENSP00000455091.1:p.Phe174=
|
|
ENST00000569684.1:n.934C>T
|
|
|
NM_000294.2:c.522C>T
|
NP_000285.1:p.Phe174=
|
|
NM_001172432.1:c.522C>T
|
NP_001165903.1:p.Phe174=
|
|
NM_000294.3:c.522C>T
MANE Select
|
NP_000285.1:p.Phe174=
|
|
NM_001172432.2:c.522C>T
|
NP_001165903.1:p.Phe174=
|
|