ENST00000209873.9:c.959C>G
MANE Select
|
ENSP00000209873.4:p.Thr320Ser
|
|
ENST00000546393.7:n.1804C>G
|
|
|
ENST00000546562.6:n.2023C>G
|
|
|
ENST00000547238.6:n.1595C>G
|
|
|
ENST00000547520.6:n.953C>G
|
|
|
ENST00000547757.2:c.8C>G
|
ENSP00000448020.2:p.Thr3Ser
|
|
ENST00000548880.2:n.1409C>G
|
|
|
ENST00000548931.6:c.479C>G
|
ENSP00000457518.1:p.Thr160Ser
|
|
ENST00000549450.6:n.893C>G
|
|
|
ENST00000552161.6:n.1915C>G
|
|
|
ENST00000672797.1:n.1412C>G
|
|
|
ENST00000672900.1:n.1757C>G
|
|
|
ENST00000209873.8:c.959C>G
|
ENSP00000209873.4:p.Thr320Ser
|
|
ENST00000394384.7:c.860C>G
|
ENSP00000377908.3:p.Thr287Ser
|
|
ENST00000546572.1:n.547C>G
|
|
|
ENST00000547520.5:n.663C>G
|
|
|
ENST00000548931.5:c.479C>G
|
ENSP00000457518.1:p.Thr160Ser
|
|
ENST00000550033.5:n.214C>G
|
|
|
ENST00000550286.5:c.587C>G
|
ENSP00000446885.1:p.Thr196Ser
|
|
ENST00000552876.5:n.1302C>G
|
|
|
NM_001173466.1:c.860C>G
|
NP_001166937.1:p.Thr287Ser
|
|
NM_015665.5:c.959C>G
|
NP_056480.1:p.Thr320Ser
|
|
XM_006719617.2:c.974C>G
|
XP_006719680.1:p.Thr325Ser
|
|
XM_006719619.2:c.974C>G
|
XP_006719682.1:p.Thr325Ser
|
|
XM_011538777.1:c.974C>G
|
XP_011537079.1:p.Thr325Ser
|
|
XM_011538778.1:c.959C>G
|
XP_011537080.1:p.Thr320Ser
|
|
XM_011538779.1:c.875C>G
|
XP_011537081.1:p.Thr292Ser
|
|
XM_011538780.1:c.860C>G
|
XP_011537082.1:p.Thr287Ser
|
|
XM_011538781.1:c.308C>G
|
XP_011537083.1:p.Thr103Ser
|
|
XM_011538778.2:c.959C>G
|
XP_011537080.1:p.Thr320Ser
|
|
XM_011538780.2:c.860C>G
|
XP_011537082.1:p.Thr287Ser
|
|
XR_001748875.2:n.980C>G
|
|
|
NM_015665.6:c.959C>G
MANE Select
|
NP_056480.1:p.Thr320Ser
|
|
NM_001173466.2:c.860C>G
|
NP_001166937.1:p.Thr287Ser
|
|