ENST00000496887.7:c.1165G=
|
ENSP00000434560.2:p.Glu389=
|
|
ENST00000646564.2:c.982G=
|
ENSP00000495806.2:p.Glu328=
|
|
ENST00000155840.12:c.1522G=
MANE Select
|
ENSP00000155840.2:p.Glu508=
|
|
ENST00000335475.6:c.1141G=
|
ENSP00000334497.5:p.Glu381=
|
|
ENST00000646564.1:c.628G=
|
ENSP00000495806.1:p.Glu210=
|
|
ENST00000155840.9:c.1522G=
|
ENSP00000155840.2:p.Glu508=
|
|
ENST00000335475.5:c.1141G=
|
ENSP00000334497.5:p.Glu381=
|
|
NM_000218.2:c.1522G= , LRG_287t1:c.1522G=
|
NP_000209.2:p.Glu508=
|
|
NM_181798.1:c.1141G= , LRG_287t2:c.1141G=
|
NP_861463.1:p.Glu381=
|
|
NM_000218.3:c.1522G=
MANE Select
|
NP_000209.2:p.Glu508=
|
|