ENST00000265343.10:c.3016G=
MANE Select
|
ENSP00000265343.5:p.Glu1006=
|
|
ENST00000265343.9:c.3016G=
|
ENSP00000265343.5:p.Glu1006=
|
|
NM_014423.3:c.3016G=
|
NP_055238.1:p.Glu1006=
|
|
XM_005271963.3:c.3016G=
|
XP_005272020.1:p.Glu1006=
|
|
XM_005271964.3:c.1882G=
|
XP_005272021.1:p.Glu628=
|
|
XM_006714587.2:c.2929G=
|
XP_006714650.1:p.Glu977=
|
|
XM_005271963.5:c.3016G=
|
XP_005272020.1:p.Glu1006=
|
|
XM_005271964.4:c.1882G=
|
XP_005272021.1:p.Glu628=
|
|
XM_006714587.4:c.2929G=
|
XP_006714650.1:p.Glu977=
|
|
NM_014423.4:c.3016G=
MANE Select
|
NP_055238.1:p.Glu1006=
|
|