ENST00000209873.9:c.1507G>T
MANE Select
|
ENSP00000209873.4:p.Glu503Ter
|
|
ENST00000546562.6:n.2571G>T
|
|
|
ENST00000547238.6:n.2143G>T
|
|
|
ENST00000547520.6:n.1623G>T
|
|
|
ENST00000547757.2:c.*425G>T
|
ENSP00000448020.2:n.*425G>T
|
|
ENST00000548931.6:c.942G>T
|
ENSP00000457518.1:p.Arg314Ser
|
|
ENST00000549450.6:n.1441G>T
|
|
|
ENST00000672797.1:n.1996G>T
|
|
|
ENST00000209873.8:c.1507G>T
|
ENSP00000209873.4:p.Glu503Ter
|
|
ENST00000394384.7:c.1408G>T
|
ENSP00000377908.3:p.Glu470Ter
|
|
ENST00000548931.5:c.942G>T
|
ENSP00000457518.1:p.Arg314Ser
|
|
ENST00000550286.5:c.1135G>T
|
ENSP00000446885.1:p.Glu379Ter
|
|
ENST00000552876.5:n.1850G>T
|
|
|
NM_001173466.1:c.1408G>T
|
NP_001166937.1:p.Glu470Ter
|
|
NM_015665.5:c.1507G>T
|
NP_056480.1:p.Glu503Ter
|
|
XM_006719617.2:c.1522G>T
|
XP_006719680.1:p.Glu508Ter
|
|
XM_011538777.1:c.1564G>T
|
XP_011537079.1:p.Glu522Ter
|
|
XM_011538778.1:c.1549G>T
|
XP_011537080.1:p.Glu517Ter
|
|
XM_011538779.1:c.1465G>T
|
XP_011537081.1:p.Glu489Ter
|
|
XM_011538780.1:c.1450G>T
|
XP_011537082.1:p.Glu484Ter
|
|
XM_011538781.1:c.898G>T
|
XP_011537083.1:p.Glu300Ter
|
|
XM_011538778.2:c.1549G>T
|
XP_011537080.1:p.Glu517Ter
|
|
XM_011538780.2:c.1450G>T
|
XP_011537082.1:p.Glu484Ter
|
|
XR_001748875.2:n.1564G>T
|
|
|
NM_015665.6:c.1507G>T
MANE Select
|
NP_056480.1:p.Glu503Ter
|
|
NM_001173466.2:c.1408G>T
|
NP_001166937.1:p.Glu470Ter
|
|