ENST00000344265.8:c.669T>C
|
ENSP00000342931.3:p.Ala223=
|
|
ENST00000350375.7:c.591T>C
MANE Select
|
ENSP00000263781.2:p.Ala197=
|
|
ENST00000344265.7:c.669T>C
|
ENSP00000342931.3:p.Ala223=
|
|
ENST00000350375.6:c.591T>C
|
ENSP00000263781.2:p.Ala197=
|
|
ENST00000560656.1:c.440-1980T>C
|
ENSP00000452610.1:n.440-1980T>C
|
|
ENST00000561167.5:c.366T>C
|
ENSP00000454072.1:p.Ala122=
|
|
NM_000306.3:c.591T>C
|
NP_000297.1:p.Ala197=
|
|
NM_001122757.2:c.669T>C
|
NP_001116229.1:p.Ala223=
|
|
NM_000306.4:c.591T>C
MANE Select
|
NP_000297.1:p.Ala197=
|
|
NM_001122757.3:c.669T>C
|
NP_001116229.1:p.Ala223=
|
|