ENST00000698881.1:c.2958G>C
|
ENSP00000514003.1:p.Glu986Asp
|
|
ENST00000418331.7:c.2616G>C
MANE Select
|
ENSP00000400010.2:p.Glu872Asp
|
|
ENST00000418331.6:c.2616G>C
|
ENSP00000400010.2:p.Glu872Asp
|
|
ENST00000613246.4:c.2616G>C
|
ENSP00000477933.1:p.Glu872Asp
|
|
ENST00000615445.4:c.2616G>C
|
ENSP00000479342.1:p.Glu872Asp
|
|
NM_002843.3:c.2616G>C
|
NP_002834.3:p.Glu872Asp
|
|
XM_011520249.1:c.2649G>C
|
XP_011518551.1:p.Glu883Asp
|
|
XR_930883.1:n.2966G>C
|
|
|
XM_017018083.1:c.2694G>C
|
XP_016873572.1:p.Glu898Asp
|
|
XM_017018084.1:c.2637G>C
|
XP_016873573.1:p.Glu879Asp
|
|
XM_017018085.1:c.2568G>C
|
XP_016873574.1:p.Glu856Asp
|
|
XR_930883.2:n.3025G>C
|
|
|
NM_002843.4:c.2616G>C
MANE Select
|
NP_002834.3:p.Glu872Asp
|
|