ENST00000209873.9:c.1017T>G
MANE Select
|
ENSP00000209873.4:p.Asp339Glu
|
|
ENST00000546393.7:n.1862T>G
|
|
|
ENST00000546562.6:n.2081T>G
|
|
|
ENST00000547238.6:n.1653T>G
|
|
|
ENST00000547520.6:n.1011T>G
|
|
|
ENST00000547757.2:c.66T>G
|
ENSP00000448020.2:p.Asp22Glu
|
|
ENST00000548880.2:n.1467T>G
|
|
|
ENST00000548931.6:c.537T>G
|
ENSP00000457518.1:p.Asp179Glu
|
|
ENST00000549450.6:n.951T>G
|
|
|
ENST00000552161.6:n.1973T>G
|
|
|
ENST00000672797.1:n.1506T>G
|
|
|
ENST00000672900.1:n.1959T>G
|
|
|
ENST00000209873.8:c.1017T>G
|
ENSP00000209873.4:p.Asp339Glu
|
|
ENST00000394384.7:c.918T>G
|
ENSP00000377908.3:p.Asp306Glu
|
|
ENST00000547520.5:n.721T>G
|
|
|
ENST00000548931.5:c.537T>G
|
ENSP00000457518.1:p.Asp179Glu
|
|
ENST00000550033.5:n.272T>G
|
|
|
ENST00000550286.5:c.645T>G
|
ENSP00000446885.1:p.Asp215Glu
|
|
ENST00000552876.5:n.1360T>G
|
|
|
NM_001173466.1:c.918T>G
|
NP_001166937.1:p.Asp306Glu
|
|
NM_015665.5:c.1017T>G
|
NP_056480.1:p.Asp339Glu
|
|
XM_006719617.2:c.1032T>G
|
XP_006719680.1:p.Asp344Glu
|
|
XM_006719619.2:c.*27T>G
|
XP_006719682.1:n.*27T>G
|
|
XM_011538777.1:c.1032T>G
|
XP_011537079.1:p.Asp344Glu
|
|
XM_011538778.1:c.1017T>G
|
XP_011537080.1:p.Asp339Glu
|
|
XM_011538779.1:c.933T>G
|
XP_011537081.1:p.Asp311Glu
|
|
XM_011538780.1:c.918T>G
|
XP_011537082.1:p.Asp306Glu
|
|
XM_011538781.1:c.366T>G
|
XP_011537083.1:p.Asp122Glu
|
|
XM_011538778.2:c.1017T>G
|
XP_011537080.1:p.Asp339Glu
|
|
XM_011538780.2:c.918T>G
|
XP_011537082.1:p.Asp306Glu
|
|
XR_001748875.2:n.1074T>G
|
|
|
NM_015665.6:c.1017T>G
MANE Select
|
NP_056480.1:p.Asp339Glu
|
|
NM_001173466.2:c.918T>G
|
NP_001166937.1:p.Asp306Glu
|
|