ENST00000209873.9:c.1071T>A
MANE Select
|
ENSP00000209873.4:p.Ser357=
|
|
ENST00000546562.6:n.2135T>A
|
|
|
ENST00000547238.6:n.1707T>A
|
|
|
ENST00000547520.6:n.1065T>A
|
|
|
ENST00000547757.2:c.120T>A
|
ENSP00000448020.2:p.Ser40=
|
|
ENST00000548880.2:n.1521T>A
|
|
|
ENST00000548931.6:c.591T>A
|
ENSP00000457518.1:p.Ser197=
|
|
ENST00000549450.6:n.1005T>A
|
|
|
ENST00000552161.6:n.2027T>A
|
|
|
ENST00000672797.1:n.1560T>A
|
|
|
ENST00000672900.1:n.2013T>A
|
|
|
ENST00000209873.8:c.1071T>A
|
ENSP00000209873.4:p.Ser357=
|
|
ENST00000394384.7:c.972T>A
|
ENSP00000377908.3:p.Ser324=
|
|
ENST00000548931.5:c.591T>A
|
ENSP00000457518.1:p.Ser197=
|
|
ENST00000550033.5:n.326T>A
|
|
|
ENST00000550286.5:c.699T>A
|
ENSP00000446885.1:p.Ser233=
|
|
ENST00000552876.5:n.1414T>A
|
|
|
NM_001173466.1:c.972T>A
|
NP_001166937.1:p.Ser324=
|
|
NM_015665.5:c.1071T>A
|
NP_056480.1:p.Ser357=
|
|
XM_006719617.2:c.1086T>A
|
XP_006719680.1:p.Ser362=
|
|
XM_011538777.1:c.1086T>A
|
XP_011537079.1:p.Ser362=
|
|
XM_011538778.1:c.1071T>A
|
XP_011537080.1:p.Ser357=
|
|
XM_011538779.1:c.987T>A
|
XP_011537081.1:p.Ser329=
|
|
XM_011538780.1:c.972T>A
|
XP_011537082.1:p.Ser324=
|
|
XM_011538781.1:c.420T>A
|
XP_011537083.1:p.Ser140=
|
|
XM_011538778.2:c.1071T>A
|
XP_011537080.1:p.Ser357=
|
|
XM_011538780.2:c.972T>A
|
XP_011537082.1:p.Ser324=
|
|
XR_001748875.2:n.1128T>A
|
|
|
NM_015665.6:c.1071T>A
MANE Select
|
NP_056480.1:p.Ser357=
|
|
NM_001173466.2:c.972T>A
|
NP_001166937.1:p.Ser324=
|
|