ENST00000305046.13:c.214G=
MANE Select
|
ENSP00000306606.8:p.Gly72=
|
|
ENST00000639454.1:c.214G=
|
ENSP00000491622.1:p.Gly72=
|
|
ENST00000305046.12:c.214G=
|
ENSP00000306606.8:p.Gly72=
|
|
ENST00000504498.1:n.268G=
|
|
|
ENST00000506651.5:c.94G=
|
ENSP00000425998.2:p.Gly32=
|
|
ENST00000515694.4:n.2309G=
|
|
|
ENST00000625860.2:c.94G=
|
ENSP00000486614.1:p.Gly32=
|
|
ENST00000632775.1:n.777G=
|
|
|
NM_000668.5:c.214G=
|
NP_000659.2:p.Gly72=
|
|
NM_001286650.1:c.94G=
|
NP_001273579.1:p.Gly32=
|
|
NM_000668.6:c.214G=
MANE Select
|
NP_000659.2:p.Gly72=
|
|
NM_001286650.2:c.94G=
|
NP_001273579.1:p.Gly32=
|
|