ENST00000622030.2:c.591G=
MANE Select
|
ENSP00000477587.1:p.Glu197=
|
|
ENST00000622030.1:c.591G=
|
ENSP00000477587.1:p.Glu197=
|
|
NM_000348.3:c.591G=
|
NP_000339.2:p.Glu197=
|
|
XM_011533069.1:c.369G=
|
XP_011531371.1:p.Glu123=
|
|
XM_011533070.1:c.336G=
|
XP_011531372.1:p.Glu112=
|
|
XM_011533071.1:c.336G=
|
XP_011531373.1:p.Glu112=
|
|
XM_011533072.1:c.336G=
|
XP_011531374.1:p.Glu112=
|
|
XM_011533069.2:c.369G=
|
XP_011531371.1:p.Glu123=
|
|
XM_011533072.2:c.336G=
|
XP_011531374.1:p.Glu112=
|
|
NM_000348.4:c.591G=
MANE Select
|
NP_000339.2:p.Glu197=
|
|