ENST00000312251.8:c.1076A>T
MANE Select
|
ENSP00000310998.3:p.Glu359Val
|
|
ENST00000649828.1:c.*248A>T
|
ENSP00000498032.1:n.*248A>T
|
|
ENST00000312251.7:c.1076A>T
|
ENSP00000310998.3:p.Glu359Val
|
|
ENST00000381955.7:c.1076A>T
|
ENSP00000371381.3:p.Glu359Val
|
|
ENST00000562746.5:c.*248A>T
|
ENSP00000455900.1:n.*248A>T
|
|
ENST00000563578.5:c.738+850A>T
|
|
|
ENST00000564397.5:n.2129A>T
|
|
|
ENST00000565876.5:c.481-651A>T
|
|
|
ENST00000566137.5:n.374A>T
|
|
|
ENST00000567739.5:n.395A>T
|
|
|
ENST00000568202.5:n.939A>T
|
|
|
ENST00000569296.5:c.689A>T
|
ENSP00000465949.1:n.689A>T
|
|
NM_016256.3:c.1076A>T
|
NP_057340.2:p.Glu359Val
|
|
XM_011522517.1:c.1076A>T
|
XP_011520819.1:p.Glu359Val
|
|
XR_243285.1:n.1172A>T
|
|
|
XM_011522517.3:c.1076A>T
|
XP_011520819.1:p.Glu359Val
|
|
XR_001751908.2:n.1171A>T
|
|
|
XR_001751909.2:n.1175A>T
|
|
|
XR_001751910.2:n.1204A>T
|
|
|
XR_001751911.2:n.1204A>T
|
|
|
XR_001751912.2:n.1208A>T
|
|
|
NM_016256.4:c.1076A>T
MANE Select
|
NP_057340.2:p.Glu359Val
|
|