ENST00000209873.9:c.1021A>T
MANE Select
|
ENSP00000209873.4:p.Ser341Cys
|
|
ENST00000546393.7:n.1866A>T
|
|
|
ENST00000546562.6:n.2085A>T
|
|
|
ENST00000547238.6:n.1657A>T
|
|
|
ENST00000547520.6:n.1015A>T
|
|
|
ENST00000547757.2:c.70A>T
|
ENSP00000448020.2:p.Ser24Cys
|
|
ENST00000548880.2:n.1471A>T
|
|
|
ENST00000548931.6:c.541A>T
|
ENSP00000457518.1:p.Ser181Cys
|
|
ENST00000549450.6:n.955A>T
|
|
|
ENST00000552161.6:n.1977A>T
|
|
|
ENST00000672797.1:n.1510A>T
|
|
|
ENST00000672900.1:n.1963A>T
|
|
|
ENST00000209873.8:c.1021A>T
|
ENSP00000209873.4:p.Ser341Cys
|
|
ENST00000394384.7:c.922A>T
|
ENSP00000377908.3:p.Ser308Cys
|
|
ENST00000547520.5:n.725A>T
|
|
|
ENST00000548931.5:c.541A>T
|
ENSP00000457518.1:p.Ser181Cys
|
|
ENST00000550033.5:n.276A>T
|
|
|
ENST00000550286.5:c.649A>T
|
ENSP00000446885.1:p.Ser217Cys
|
|
ENST00000552876.5:n.1364A>T
|
|
|
NM_001173466.1:c.922A>T
|
NP_001166937.1:p.Ser308Cys
|
|
NM_015665.5:c.1021A>T
|
NP_056480.1:p.Ser341Cys
|
|
XM_006719617.2:c.1036A>T
|
XP_006719680.1:p.Ser346Cys
|
|
XM_006719619.2:c.*31A>T
|
XP_006719682.1:n.*31A>T
|
|
XM_011538777.1:c.1036A>T
|
XP_011537079.1:p.Ser346Cys
|
|
XM_011538778.1:c.1021A>T
|
XP_011537080.1:p.Ser341Cys
|
|
XM_011538779.1:c.937A>T
|
XP_011537081.1:p.Ser313Cys
|
|
XM_011538780.1:c.922A>T
|
XP_011537082.1:p.Ser308Cys
|
|
XM_011538781.1:c.370A>T
|
XP_011537083.1:p.Ser124Cys
|
|
XM_011538778.2:c.1021A>T
|
XP_011537080.1:p.Ser341Cys
|
|
XM_011538780.2:c.922A>T
|
XP_011537082.1:p.Ser308Cys
|
|
XR_001748875.2:n.1078A>T
|
|
|
NM_015665.6:c.1021A>T
MANE Select
|
NP_056480.1:p.Ser341Cys
|
|
NM_001173466.2:c.922A>T
|
NP_001166937.1:p.Ser308Cys
|
|