ENST00000380036.10:c.2763G>A
MANE Select
|
ENSP00000369375.4:p.Glu921=
|
|
ENST00000380036.8:c.2763G>A
|
ENSP00000369375.4:p.Glu921=
|
|
ENST00000406359.8:c.2634G>A
|
ENSP00000383977.4:p.Glu878=
|
|
ENST00000519097.5:c.2319G>A
|
ENSP00000430686.1:p.Glu773=
|
|
ENST00000615002.4:c.*1264G>A
|
ENSP00000480251.1:n.*1264G>A
|
|
NM_000459.4:c.2763G>A
|
NP_000450.2:p.Glu921=
|
|
NM_001290077.1:c.2634G>A
|
NP_001277006.1:p.Glu878=
|
|
NM_001290078.1:c.2319G>A
|
NP_001277007.1:p.Glu773=
|
|
XM_005251561.1:c.2760G>A
|
XP_005251618.1:p.Glu920=
|
|
XM_005251563.1:c.2631G>A
|
XP_005251620.1:p.Glu877=
|
|
XM_005251561.2:c.2760G>A
|
XP_005251618.1:p.Glu920=
|
|
XM_005251563.2:c.2631G>A
|
XP_005251620.1:p.Glu877=
|
|
NM_000459.5:c.2763G>A
MANE Select
|
NP_000450.3:p.Glu921=
|
|
NM_001375475.1:c.2760G>A
|
NP_001362404.1:p.Glu920=
|
|
NM_001375476.1:c.2631G>A
|
NP_001362405.1:p.Glu877=
|
|