NM_000417.3:c.692A=
MANE Select
|
NP_000408.1:p.Glu231=
|
ENST00000379959.8:c.692A=
MANE Select
|
ENSP00000369293.3:p.Glu231=
|
NM_000417.2:c.692A= , LRG_73t1:c.692A=
|
NP_000408.1:p.Glu231=
|
NM_001308242.1:c.476A=
|
NP_001295171.1:p.Glu159=
|
NM_001308242.2:c.476A=
|
NP_001295171.1:p.Glu159=
|
NM_001308243.1:c.404A=
|
NP_001295172.1:p.Glu135=
|
NM_001308243.2:c.404A=
|
NP_001295172.1:p.Glu135=
|
ENST00000256876.10:c.665A=
|
ENSP00000256876.6:p.Glu222=
|
ENST00000379954.5:c.476A=
|
ENSP00000369287.1:p.Glu159=
|
ENST00000379959.7:c.692A=
|
ENSP00000369293.3:p.Glu231=
|
ENST00000447847.1:c.316A=
|
|
ENST00000447847.2:c.404A=
|
ENSP00000402024.2:p.Glu135=
|
ENST00000649218.1:n.507A=
|
|
ENST00000697424.1:c.620A=
|
ENSP00000513307.1:p.Glu207=
|