ENST00000330342.8:c.1354T>G
MANE Select
|
ENSP00000332247.2:p.Tyr452Asp
|
|
ENST00000540368.6:n.1385T>G
|
|
|
ENST00000674794.1:c.1442T>G
|
|
|
ENST00000675260.1:n.629T>G
|
|
|
ENST00000675344.1:c.*375T>G
|
ENSP00000501953.1:n.*375T>G
|
|
ENST00000330342.7:c.1354T>G
|
ENSP00000332247.2:p.Tyr452Asp
|
|
ENST00000504192.2:c.964T>G
|
ENSP00000443441.1:p.Tyr322Asp
|
|
ENST00000536426.1:n.371T>G
|
|
|
ENST00000545059.5:n.3990T>G
|
|
|
NM_012463.3:c.1354T>G
|
NP_036595.2:p.Tyr452Asp
|
|
XM_005253563.1:c.1354T>G
|
XP_005253620.1:p.Tyr452Asp
|
|
XM_006719317.2:c.841T>G
|
XP_006719380.1:p.Tyr281Asp
|
|
XM_006719318.2:c.532T>G
|
XP_006719381.1:p.Tyr178Asp
|
|
XR_429088.1:n.1517T>G
|
|
|
XM_024448910.1:c.1354T>G
|
XP_024304678.1:p.Tyr452Asp
|
|
XM_024448911.1:c.841T>G
|
XP_024304679.1:p.Tyr281Asp
|
|
XM_024448912.1:c.532T>G
|
XP_024304680.1:p.Tyr178Asp
|
|
NM_012463.4:c.1354T>G
MANE Select
|
NP_036595.2:p.Tyr452Asp
|
|