ENST00000209873.9:c.1079A>T
MANE Select
|
ENSP00000209873.4:p.Glu360Val
|
|
ENST00000546562.6:n.2143A>T
|
|
|
ENST00000547238.6:n.1715A>T
|
|
|
ENST00000547520.6:n.1073A>T
|
|
|
ENST00000547757.2:c.128A>T
|
ENSP00000448020.2:p.Glu43Val
|
|
ENST00000548880.2:n.1529A>T
|
|
|
ENST00000548931.6:c.599A>T
|
ENSP00000457518.1:p.Glu200Val
|
|
ENST00000549450.6:n.1013A>T
|
|
|
ENST00000552161.6:n.2035A>T
|
|
|
ENST00000672797.1:n.1568A>T
|
|
|
ENST00000672900.1:n.2021A>T
|
|
|
ENST00000209873.8:c.1079A>T
|
ENSP00000209873.4:p.Glu360Val
|
|
ENST00000394384.7:c.980A>T
|
ENSP00000377908.3:p.Glu327Val
|
|
ENST00000548931.5:c.599A>T
|
ENSP00000457518.1:p.Glu200Val
|
|
ENST00000550033.5:n.334A>T
|
|
|
ENST00000550286.5:c.707A>T
|
ENSP00000446885.1:p.Glu236Val
|
|
ENST00000552876.5:n.1422A>T
|
|
|
NM_001173466.1:c.980A>T
|
NP_001166937.1:p.Glu327Val
|
|
NM_015665.5:c.1079A>T
|
NP_056480.1:p.Glu360Val
|
|
XM_006719617.2:c.1094A>T
|
XP_006719680.1:p.Glu365Val
|
|
XM_011538777.1:c.1094A>T
|
XP_011537079.1:p.Glu365Val
|
|
XM_011538778.1:c.1079A>T
|
XP_011537080.1:p.Glu360Val
|
|
XM_011538779.1:c.995A>T
|
XP_011537081.1:p.Glu332Val
|
|
XM_011538780.1:c.980A>T
|
XP_011537082.1:p.Glu327Val
|
|
XM_011538781.1:c.428A>T
|
XP_011537083.1:p.Glu143Val
|
|
XM_011538778.2:c.1079A>T
|
XP_011537080.1:p.Glu360Val
|
|
XM_011538780.2:c.980A>T
|
XP_011537082.1:p.Glu327Val
|
|
XR_001748875.2:n.1136A>T
|
|
|
NM_015665.6:c.1079A>T
MANE Select
|
NP_056480.1:p.Glu360Val
|
|
NM_001173466.2:c.980A>T
|
NP_001166937.1:p.Glu327Val
|
|