ENST00000344265.8:c.840G>A
|
ENSP00000342931.3:p.Glu280=
|
|
ENST00000350375.7:c.762G>A
MANE Select
|
ENSP00000263781.2:p.Glu254=
|
|
ENST00000344265.7:c.840G>A
|
ENSP00000342931.3:p.Glu280=
|
|
ENST00000350375.6:c.762G>A
|
ENSP00000263781.2:p.Glu254=
|
|
ENST00000560656.1:c.536G>A
|
ENSP00000452610.1:n.536G>A
|
|
ENST00000561167.5:c.537G>A
|
ENSP00000454072.1:p.Glu179=
|
|
NM_000306.3:c.762G>A
|
NP_000297.1:p.Glu254=
|
|
NM_001122757.2:c.840G>A
|
NP_001116229.1:p.Glu280=
|
|
NM_000306.4:c.762G>A
MANE Select
|
NP_000297.1:p.Glu254=
|
|
NM_001122757.3:c.840G>A
|
NP_001116229.1:p.Glu280=
|
|