ENST00000344265.8:c.859T>C
|
ENSP00000342931.3:p.Trp287Arg
|
|
ENST00000350375.7:c.781T>C
MANE Select
|
ENSP00000263781.2:p.Trp261Arg
|
|
ENST00000344265.7:c.859T>C
|
ENSP00000342931.3:p.Trp287Arg
|
|
ENST00000350375.6:c.781T>C
|
ENSP00000263781.2:p.Trp261Arg
|
|
ENST00000560656.1:c.555T>C
|
ENSP00000452610.1:n.555T>C
|
|
ENST00000561167.5:c.556T>C
|
ENSP00000454072.1:p.Trp186Arg
|
|
NM_000306.3:c.781T>C
|
NP_000297.1:p.Trp261Arg
|
|
NM_001122757.2:c.859T>C
|
NP_001116229.1:p.Trp287Arg
|
|
NM_000306.4:c.781T>C
MANE Select
|
NP_000297.1:p.Trp261Arg
|
|
NM_001122757.3:c.859T>C
|
NP_001116229.1:p.Trp287Arg
|
|