ENST00000269980.7:c.869G=
MANE Select
|
ENSP00000269980.2:p.Gly290=
|
|
ENST00000269980.6:c.869G=
|
ENSP00000269980.2:p.Gly290=
|
|
ENST00000457836.6:c.803G=
|
ENSP00000416000.2:p.Gly268=
|
|
ENST00000535632.5:n.498G=
|
|
|
ENST00000540732.3:c.971G=
|
ENSP00000443246.1:p.Gly324=
|
|
ENST00000542943.5:c.782G=
|
ENSP00000440345.1:p.Gly261=
|
|
ENST00000545787.1:n.497G=
|
|
|
ENST00000595085.5:c.869G=
|
ENSP00000471150.2:p.Gly290=
|
|
NM_000709.3:c.869G=
|
NP_000700.1:p.Gly290=
|
|
NM_001164783.1:c.866G=
|
NP_001158255.1:p.Gly289=
|
|
NM_000709.4:c.869G=
MANE Select
|
NP_000700.1:p.Gly290=
|
|
NM_001164783.2:c.866G=
|
NP_001158255.1:p.Gly289=
|
|