ENST00000496887.7:c.1176G=
|
ENSP00000434560.2:p.Arg392=
|
|
ENST00000646564.2:c.993G=
|
ENSP00000495806.2:p.Arg331=
|
|
ENST00000155840.12:c.1533G=
MANE Select
|
ENSP00000155840.2:p.Arg511=
|
|
ENST00000335475.6:c.1152G=
|
ENSP00000334497.5:p.Arg384=
|
|
ENST00000646564.1:c.639G=
|
ENSP00000495806.1:p.Arg213=
|
|
ENST00000155840.9:c.1533G=
|
ENSP00000155840.2:p.Arg511=
|
|
ENST00000335475.5:c.1152G=
|
ENSP00000334497.5:p.Arg384=
|
|
NM_000218.2:c.1533G= , LRG_287t1:c.1533G=
|
NP_000209.2:p.Arg511=
|
|
NM_181798.1:c.1152G= , LRG_287t2:c.1152G=
|
NP_861463.1:p.Arg384=
|
|
NM_000218.3:c.1533G=
MANE Select
|
NP_000209.2:p.Arg511=
|
|