ENST00000209873.9:c.1010G>C
MANE Select
|
ENSP00000209873.4:p.Ser337Thr
|
|
ENST00000546393.7:n.1855G>C
|
|
|
ENST00000546562.6:n.2074G>C
|
|
|
ENST00000547238.6:n.1646G>C
|
|
|
ENST00000547520.6:n.1004G>C
|
|
|
ENST00000547757.2:c.59G>C
|
ENSP00000448020.2:p.Ser20Thr
|
|
ENST00000548880.2:n.1460G>C
|
|
|
ENST00000548931.6:c.530G>C
|
ENSP00000457518.1:p.Ser177Thr
|
|
ENST00000549450.6:n.944G>C
|
|
|
ENST00000552161.6:n.1966G>C
|
|
|
ENST00000672797.1:n.1499G>C
|
|
|
ENST00000672900.1:n.1952G>C
|
|
|
ENST00000209873.8:c.1010G>C
|
ENSP00000209873.4:p.Ser337Thr
|
|
ENST00000394384.7:c.911G>C
|
ENSP00000377908.3:p.Ser304Thr
|
|
ENST00000547520.5:n.714G>C
|
|
|
ENST00000548931.5:c.530G>C
|
ENSP00000457518.1:p.Ser177Thr
|
|
ENST00000550033.5:n.265G>C
|
|
|
ENST00000550286.5:c.638G>C
|
ENSP00000446885.1:p.Ser213Thr
|
|
ENST00000552876.5:n.1353G>C
|
|
|
NM_001173466.1:c.911G>C
|
NP_001166937.1:p.Ser304Thr
|
|
NM_015665.5:c.1010G>C
|
NP_056480.1:p.Ser337Thr
|
|
XM_006719617.2:c.1025G>C
|
XP_006719680.1:p.Ser342Thr
|
|
XM_006719619.2:c.*20G>C
|
XP_006719682.1:n.*20G>C
|
|
XM_011538777.1:c.1025G>C
|
XP_011537079.1:p.Ser342Thr
|
|
XM_011538778.1:c.1010G>C
|
XP_011537080.1:p.Ser337Thr
|
|
XM_011538779.1:c.926G>C
|
XP_011537081.1:p.Ser309Thr
|
|
XM_011538780.1:c.911G>C
|
XP_011537082.1:p.Ser304Thr
|
|
XM_011538781.1:c.359G>C
|
XP_011537083.1:p.Ser120Thr
|
|
XM_011538778.2:c.1010G>C
|
XP_011537080.1:p.Ser337Thr
|
|
XM_011538780.2:c.911G>C
|
XP_011537082.1:p.Ser304Thr
|
|
XR_001748875.2:n.1067G>C
|
|
|
NM_015665.6:c.1010G>C
MANE Select
|
NP_056480.1:p.Ser337Thr
|
|
NM_001173466.2:c.911G>C
|
NP_001166937.1:p.Ser304Thr
|
|