ENST00000337554.8:c.489G=
MANE Select
|
ENSP00000338004.3:p.Gly163=
|
|
ENST00000329563.8:c.489G=
|
ENSP00000328973.4:p.Gly163=
|
|
ENST00000337554.7:c.489G=
|
ENSP00000338004.3:p.Gly163=
|
|
ENST00000396265.4:c.489G=
|
ENSP00000379563.4:p.Gly163=
|
|
ENST00000583777.5:c.177G=
|
ENSP00000463495.1:p.Gly59=
|
|
NM_000714.5:c.489G=
|
NP_000705.2:p.Gly163=
|
|
NM_001256530.1:c.489G=
|
NP_001243459.1:p.Gly163=
|
|
NM_001256531.1:c.489G=
|
NP_001243460.1:p.Gly163=
|
|
NR_046308.1:n.398G=
|
|
|
NM_000714.6:c.489G=
MANE Select
|
NP_000705.2:p.Gly163=
|
|
NR_046308.2:n.353G=
|
|
|