ENST00000496887.7:c.712G=
|
ENSP00000434560.2:p.Gly238=
|
|
ENST00000646564.2:c.529G=
|
ENSP00000495806.2:p.Gly177=
|
|
ENST00000155840.12:c.973G=
MANE Select
|
ENSP00000155840.2:p.Gly325=
|
|
ENST00000335475.6:c.592G=
|
ENSP00000334497.5:p.Gly198=
|
|
ENST00000646564.1:c.175G=
|
ENSP00000495806.1:p.Gly59=
|
|
ENST00000155840.9:c.973G=
|
ENSP00000155840.2:p.Gly325=
|
|
ENST00000335475.5:c.592G=
|
ENSP00000334497.5:p.Gly198=
|
|
NM_000218.2:c.973G= , LRG_287t1:c.973G=
|
NP_000209.2:p.Gly325=
|
|
NM_181798.1:c.592G= , LRG_287t2:c.592G=
|
NP_861463.1:p.Gly198=
|
|
NM_000218.3:c.973G=
MANE Select
|
NP_000209.2:p.Gly325=
|
|