ENST00000368485.8:c.951A>C
MANE Select
|
ENSP00000357470.3:p.Glu317Asp
|
|
ENST00000344086.8:c.951A>C
|
ENSP00000340589.4:p.Glu317Asp
|
|
ENST00000368485.7:c.951A>C
|
ENSP00000357470.3:p.Glu317Asp
|
|
ENST00000476006.5:c.767A>C
|
|
|
ENST00000507256.1:n.149A>C
|
|
|
ENST00000515190.1:c.359A>C
|
|
|
NM_000565.3:c.951A>C
|
NP_000556.1:p.Glu317Asp
|
|
NM_181359.2:c.951A>C
|
NP_852004.1:p.Glu317Asp
|
|
XM_005245139.1:c.809A>C
|
XP_005245196.1:p.Asn270Thr
|
|
XM_005245140.1:c.809A>C
|
XP_005245197.1:p.Asn270Thr
|
|
XM_006711298.1:c.999A>C
|
XP_006711361.1:p.Glu333Asp
|
|
XM_006711299.2:c.999A>C
|
XP_006711362.1:p.Glu333Asp
|
|
XM_005245139.2:c.809A>C
|
XP_005245196.1:p.Asn270Thr
|
|
XM_005245140.3:c.809A>C
|
XP_005245197.1:p.Asn270Thr
|
|
XM_006711298.2:c.999A>C
|
XP_006711361.1:p.Glu333Asp
|
|
XM_006711299.4:c.999A>C
|
XP_006711362.1:p.Glu333Asp
|
|
XM_017001199.2:c.999A>C
|
XP_016856688.1:p.Glu333Asp
|
|
XM_017001200.2:c.951A>C
|
XP_016856689.1:p.Glu317Asp
|
|
XM_017001201.2:c.809A>C
|
XP_016856690.1:p.Asn270Thr
|
|
NM_000565.4:c.951A>C
MANE Select
|
NP_000556.1:p.Glu317Asp
|
|
NM_181359.3:c.951A>C
|
NP_852004.1:p.Glu317Asp
|
|
NM_001382769.1:c.951A>C
|
NP_001369698.1:p.Glu317Asp
|
|
NM_001382770.1:c.1044A>C
|
NP_001369699.1:p.Glu348Asp
|
|
NM_001382771.1:c.999A>C
|
NP_001369700.1:p.Glu333Asp
|
|
NM_001382772.1:c.945A>C
|
NP_001369701.1:p.Glu315Asp
|
|
NM_001382773.1:c.999A>C
|
NP_001369702.1:p.Glu333Asp
|
|
NM_001382774.1:c.591A>C
|
NP_001369703.1:p.Glu197Asp
|
|