ENST00000209873.9:c.1455C>G
MANE Select
|
ENSP00000209873.4:p.Tyr485Ter
|
|
ENST00000546562.6:n.2519C>G
|
|
|
ENST00000547238.6:n.2091C>G
|
|
|
ENST00000547520.6:n.1571C>G
|
|
|
ENST00000547757.2:c.*373C>G
|
ENSP00000448020.2:n.*373C>G
|
|
ENST00000548880.2:n.1905C>G
|
|
|
ENST00000548931.6:c.890C>G
|
ENSP00000457518.1:p.Thr297Ser
|
|
ENST00000549450.6:n.1389C>G
|
|
|
ENST00000552161.6:n.2533C>G
|
|
|
ENST00000672797.1:n.1944C>G
|
|
|
ENST00000209873.8:c.1455C>G
|
ENSP00000209873.4:p.Tyr485Ter
|
|
ENST00000394384.7:c.1356C>G
|
ENSP00000377908.3:p.Tyr452Ter
|
|
ENST00000548931.5:c.890C>G
|
ENSP00000457518.1:p.Thr297Ser
|
|
ENST00000550286.5:c.1083C>G
|
ENSP00000446885.1:p.Tyr361Ter
|
|
ENST00000552876.5:n.1798C>G
|
|
|
NM_001173466.1:c.1356C>G
|
NP_001166937.1:p.Tyr452Ter
|
|
NM_015665.5:c.1455C>G
|
NP_056480.1:p.Tyr485Ter
|
|
XM_006719617.2:c.1470C>G
|
XP_006719680.1:p.Tyr490Ter
|
|
XM_011538777.1:c.1512C>G
|
XP_011537079.1:p.Tyr504Ter
|
|
XM_011538778.1:c.1497C>G
|
XP_011537080.1:p.Tyr499Ter
|
|
XM_011538779.1:c.1413C>G
|
XP_011537081.1:p.Tyr471Ter
|
|
XM_011538780.1:c.1398C>G
|
XP_011537082.1:p.Tyr466Ter
|
|
XM_011538781.1:c.846C>G
|
XP_011537083.1:p.Tyr282Ter
|
|
XM_011538778.2:c.1497C>G
|
XP_011537080.1:p.Tyr499Ter
|
|
XM_011538780.2:c.1398C>G
|
XP_011537082.1:p.Tyr466Ter
|
|
XR_001748875.2:n.1512C>G
|
|
|
NM_015665.6:c.1455C>G
MANE Select
|
NP_056480.1:p.Tyr485Ter
|
|
NM_001173466.2:c.1356C>G
|
NP_001166937.1:p.Tyr452Ter
|
|