ENST00000209873.9:c.1036A>T
MANE Select
|
ENSP00000209873.4:p.Thr346Ser
|
|
ENST00000546393.7:n.1881A>T
|
|
|
ENST00000546562.6:n.2100A>T
|
|
|
ENST00000547238.6:n.1672A>T
|
|
|
ENST00000547520.6:n.1030A>T
|
|
|
ENST00000547757.2:c.85A>T
|
ENSP00000448020.2:p.Thr29Ser
|
|
ENST00000548880.2:n.1486A>T
|
|
|
ENST00000548931.6:c.556A>T
|
ENSP00000457518.1:p.Thr186Ser
|
|
ENST00000549450.6:n.970A>T
|
|
|
ENST00000552161.6:n.1992A>T
|
|
|
ENST00000672797.1:n.1525A>T
|
|
|
ENST00000672900.1:n.1978A>T
|
|
|
ENST00000209873.8:c.1036A>T
|
ENSP00000209873.4:p.Thr346Ser
|
|
ENST00000394384.7:c.937A>T
|
ENSP00000377908.3:p.Thr313Ser
|
|
ENST00000547520.5:n.740A>T
|
|
|
ENST00000548931.5:c.556A>T
|
ENSP00000457518.1:p.Thr186Ser
|
|
ENST00000550033.5:n.291A>T
|
|
|
ENST00000550286.5:c.664A>T
|
ENSP00000446885.1:p.Thr222Ser
|
|
ENST00000552876.5:n.1379A>T
|
|
|
NM_001173466.1:c.937A>T
|
NP_001166937.1:p.Thr313Ser
|
|
NM_015665.5:c.1036A>T
|
NP_056480.1:p.Thr346Ser
|
|
XM_006719617.2:c.1051A>T
|
XP_006719680.1:p.Thr351Ser
|
|
XM_006719619.2:c.*46A>T
|
XP_006719682.1:n.*46A>T
|
|
XM_011538777.1:c.1051A>T
|
XP_011537079.1:p.Thr351Ser
|
|
XM_011538778.1:c.1036A>T
|
XP_011537080.1:p.Thr346Ser
|
|
XM_011538779.1:c.952A>T
|
XP_011537081.1:p.Thr318Ser
|
|
XM_011538780.1:c.937A>T
|
XP_011537082.1:p.Thr313Ser
|
|
XM_011538781.1:c.385A>T
|
XP_011537083.1:p.Thr129Ser
|
|
XM_011538778.2:c.1036A>T
|
XP_011537080.1:p.Thr346Ser
|
|
XM_011538780.2:c.937A>T
|
XP_011537082.1:p.Thr313Ser
|
|
XR_001748875.2:n.1093A>T
|
|
|
NM_015665.6:c.1036A>T
MANE Select
|
NP_056480.1:p.Thr346Ser
|
|
NM_001173466.2:c.937A>T
|
NP_001166937.1:p.Thr313Ser
|
|