ENST00000209873.9:c.1080A>T
MANE Select
|
ENSP00000209873.4:p.Glu360Asp
|
|
ENST00000546562.6:n.2144A>T
|
|
|
ENST00000547238.6:n.1716A>T
|
|
|
ENST00000547520.6:n.1074A>T
|
|
|
ENST00000547757.2:c.129A>T
|
ENSP00000448020.2:p.Glu43Asp
|
|
ENST00000548880.2:n.1530A>T
|
|
|
ENST00000548931.6:c.600A>T
|
ENSP00000457518.1:p.Glu200Asp
|
|
ENST00000549450.6:n.1014A>T
|
|
|
ENST00000552161.6:n.2036A>T
|
|
|
ENST00000672797.1:n.1569A>T
|
|
|
ENST00000672900.1:n.2022A>T
|
|
|
ENST00000209873.8:c.1080A>T
|
ENSP00000209873.4:p.Glu360Asp
|
|
ENST00000394384.7:c.981A>T
|
ENSP00000377908.3:p.Glu327Asp
|
|
ENST00000548931.5:c.600A>T
|
ENSP00000457518.1:p.Glu200Asp
|
|
ENST00000550033.5:n.335A>T
|
|
|
ENST00000550286.5:c.708A>T
|
ENSP00000446885.1:p.Glu236Asp
|
|
ENST00000552876.5:n.1423A>T
|
|
|
NM_001173466.1:c.981A>T
|
NP_001166937.1:p.Glu327Asp
|
|
NM_015665.5:c.1080A>T
|
NP_056480.1:p.Glu360Asp
|
|
XM_006719617.2:c.1095A>T
|
XP_006719680.1:p.Glu365Asp
|
|
XM_011538777.1:c.1095A>T
|
XP_011537079.1:p.Glu365Asp
|
|
XM_011538778.1:c.1080A>T
|
XP_011537080.1:p.Glu360Asp
|
|
XM_011538779.1:c.996A>T
|
XP_011537081.1:p.Glu332Asp
|
|
XM_011538780.1:c.981A>T
|
XP_011537082.1:p.Glu327Asp
|
|
XM_011538781.1:c.429A>T
|
XP_011537083.1:p.Glu143Asp
|
|
XM_011538778.2:c.1080A>T
|
XP_011537080.1:p.Glu360Asp
|
|
XM_011538780.2:c.981A>T
|
XP_011537082.1:p.Glu327Asp
|
|
XR_001748875.2:n.1137A>T
|
|
|
NM_015665.6:c.1080A>T
MANE Select
|
NP_056480.1:p.Glu360Asp
|
|
NM_001173466.2:c.981A>T
|
NP_001166937.1:p.Glu327Asp
|
|