ENST00000209873.9:c.1496G>T
MANE Select
|
ENSP00000209873.4:p.Gly499Val
|
|
ENST00000546562.6:n.2560G>T
|
|
|
ENST00000547238.6:n.2132G>T
|
|
|
ENST00000547520.6:n.1612G>T
|
|
|
ENST00000547757.2:c.*414G>T
|
ENSP00000448020.2:n.*414G>T
|
|
ENST00000548931.6:c.931G>T
|
ENSP00000457518.1:p.Gly311Cys
|
|
ENST00000549450.6:n.1430G>T
|
|
|
ENST00000672797.1:n.1985G>T
|
|
|
ENST00000209873.8:c.1496G>T
|
ENSP00000209873.4:p.Gly499Val
|
|
ENST00000394384.7:c.1397G>T
|
ENSP00000377908.3:p.Gly466Val
|
|
ENST00000548931.5:c.931G>T
|
ENSP00000457518.1:p.Gly311Cys
|
|
ENST00000550286.5:c.1124G>T
|
ENSP00000446885.1:p.Gly375Val
|
|
ENST00000552876.5:n.1839G>T
|
|
|
NM_001173466.1:c.1397G>T
|
NP_001166937.1:p.Gly466Val
|
|
NM_015665.5:c.1496G>T
|
NP_056480.1:p.Gly499Val
|
|
XM_006719617.2:c.1511G>T
|
XP_006719680.1:p.Gly504Val
|
|
XM_011538777.1:c.1553G>T
|
XP_011537079.1:p.Gly518Val
|
|
XM_011538778.1:c.1538G>T
|
XP_011537080.1:p.Gly513Val
|
|
XM_011538779.1:c.1454G>T
|
XP_011537081.1:p.Gly485Val
|
|
XM_011538780.1:c.1439G>T
|
XP_011537082.1:p.Gly480Val
|
|
XM_011538781.1:c.887G>T
|
XP_011537083.1:p.Gly296Val
|
|
XM_011538778.2:c.1538G>T
|
XP_011537080.1:p.Gly513Val
|
|
XM_011538780.2:c.1439G>T
|
XP_011537082.1:p.Gly480Val
|
|
XR_001748875.2:n.1553G>T
|
|
|
NM_015665.6:c.1496G>T
MANE Select
|
NP_056480.1:p.Gly499Val
|
|
NM_001173466.2:c.1397G>T
|
NP_001166937.1:p.Gly466Val
|
|