ENST00000563588.6:c.766G=
MANE Select
|
ENSP00000455607.1:p.Glu256=
|
|
ENST00000328273.11:c.778G=
|
ENSP00000329968.7:p.Glu260=
|
|
ENST00000424889.7:c.766G=
|
ENSP00000388571.3:p.Glu256=
|
|
ENST00000563588.5:c.766G=
|
ENSP00000455607.1:p.Glu256=
|
|
ENST00000563913.5:n.1099G=
|
|
|
ENST00000564838.5:n.931-105G=
|
|
|
ENST00000565897.5:c.766G=
|
ENSP00000457359.1:p.Glu256=
|
|
NM_000294.2:c.766G=
|
NP_000285.1:p.Glu256=
|
|
NM_001172432.1:c.766G=
|
NP_001165903.1:p.Glu256=
|
|
NM_000294.3:c.766G=
MANE Select
|
NP_000285.1:p.Glu256=
|
|
NM_001172432.2:c.766G=
|
NP_001165903.1:p.Glu256=
|
|