ENST00000344265.8:c.809T=
|
ENSP00000342931.3:p.Ile270=
|
|
ENST00000350375.7:c.731T=
MANE Select
|
ENSP00000263781.2:p.Ile244=
|
|
ENST00000344265.7:c.809T=
|
ENSP00000342931.3:p.Ile270=
|
|
ENST00000350375.6:c.731T=
|
ENSP00000263781.2:p.Ile244=
|
|
ENST00000560656.1:c.505T=
|
ENSP00000452610.1:p.Ser169=
|
|
ENST00000561167.5:c.506T=
|
ENSP00000454072.1:p.Ile169=
|
|
NM_000306.3:c.731T=
|
NP_000297.1:p.Ile244=
|
|
NM_001122757.2:c.809T=
|
NP_001116229.1:p.Ile270=
|
|
NM_000306.4:c.731T=
MANE Select
|
NP_000297.1:p.Ile244=
|
|
NM_001122757.3:c.809T=
|
NP_001116229.1:p.Ile270=
|
|