ENST00000330342.8:c.1356C>T
MANE Select
|
ENSP00000332247.2:p.Tyr452=
|
|
ENST00000540368.6:n.1387C>T
|
|
|
ENST00000674794.1:c.1444C>T
|
|
|
ENST00000675260.1:n.631C>T
|
|
|
ENST00000675344.1:c.*377C>T
|
ENSP00000501953.1:n.*377C>T
|
|
ENST00000330342.7:c.1356C>T
|
ENSP00000332247.2:p.Tyr452=
|
|
ENST00000504192.2:c.966C>T
|
ENSP00000443441.1:p.Tyr322=
|
|
ENST00000536426.1:n.373C>T
|
|
|
ENST00000545059.5:n.3992C>T
|
|
|
NM_012463.3:c.1356C>T
|
NP_036595.2:p.Tyr452=
|
|
XM_005253563.1:c.1356C>T
|
XP_005253620.1:p.Tyr452=
|
|
XM_006719317.2:c.843C>T
|
XP_006719380.1:p.Tyr281=
|
|
XM_006719318.2:c.534C>T
|
XP_006719381.1:p.Tyr178=
|
|
XR_429088.1:n.1519C>T
|
|
|
XM_024448910.1:c.1356C>T
|
XP_024304678.1:p.Tyr452=
|
|
XM_024448911.1:c.843C>T
|
XP_024304679.1:p.Tyr281=
|
|
XM_024448912.1:c.534C>T
|
XP_024304680.1:p.Tyr178=
|
|
NM_012463.4:c.1356C>T
MANE Select
|
NP_036595.2:p.Tyr452=
|
|