ENST00000496887.7:c.783G=
|
ENSP00000434560.2:p.Arg261=
|
|
ENST00000646564.2:c.600G=
|
ENSP00000495806.2:p.Arg200=
|
|
ENST00000155840.12:c.1140G=
MANE Select
|
ENSP00000155840.2:p.Arg380=
|
|
ENST00000335475.6:c.759G=
|
ENSP00000334497.5:p.Arg253=
|
|
ENST00000646564.1:c.246G=
|
ENSP00000495806.1:p.Arg82=
|
|
ENST00000155840.9:c.1140G=
|
ENSP00000155840.2:p.Arg380=
|
|
ENST00000335475.5:c.759G=
|
ENSP00000334497.5:p.Arg253=
|
|
NM_000218.2:c.1140G= , LRG_287t1:c.1140G=
|
NP_000209.2:p.Arg380=
|
|
NM_181798.1:c.759G= , LRG_287t2:c.759G=
|
NP_861463.1:p.Arg253=
|
|
NM_000218.3:c.1140G=
MANE Select
|
NP_000209.2:p.Arg380=
|
|