ENST00000698881.1:c.2958G>A
|
ENSP00000514003.1:p.Glu986=
|
|
ENST00000418331.7:c.2616G>A
MANE Select
|
ENSP00000400010.2:p.Glu872=
|
|
ENST00000418331.6:c.2616G>A
|
ENSP00000400010.2:p.Glu872=
|
|
ENST00000613246.4:c.2616G>A
|
ENSP00000477933.1:p.Glu872=
|
|
ENST00000615445.4:c.2616G>A
|
ENSP00000479342.1:p.Glu872=
|
|
NM_002843.3:c.2616G>A
|
NP_002834.3:p.Glu872=
|
|
XM_011520249.1:c.2649G>A
|
XP_011518551.1:p.Glu883=
|
|
XR_930883.1:n.2966G>A
|
|
|
XM_017018083.1:c.2694G>A
|
XP_016873572.1:p.Glu898=
|
|
XM_017018084.1:c.2637G>A
|
XP_016873573.1:p.Glu879=
|
|
XM_017018085.1:c.2568G>A
|
XP_016873574.1:p.Glu856=
|
|
XR_930883.2:n.3025G>A
|
|
|
NM_002843.4:c.2616G>A
MANE Select
|
NP_002834.3:p.Glu872=
|
|