NM_002334.4:c.3697G=
MANE Select
|
NP_002325.2:p.Glu1233=
|
ENST00000378623.6:c.3697G=
MANE Select
|
ENSP00000367888.1:p.Glu1233=
|
NM_002334.3:c.3697G=
|
NP_002325.2:p.Glu1233=
|
ENST00000378623.5:c.3697G=
|
ENSP00000367888.1:p.Glu1233=
|
XM_011520102.1:c.3910G=
|
XP_011518404.1:p.Glu1304=
|
XM_011520103.1:c.2893G=
|
XP_011518405.1:p.Glu965=
|
XM_011520103.2:c.2893G=
|
XP_011518405.1:p.Glu965=
|
XM_011520104.1:c.1462G=
|
XP_011518406.1:p.Glu488=
|
XM_011520104.2:c.1462G=
|
XP_011518406.1:p.Glu488=
|
XM_017017734.1:c.3697G=
|
XP_016873223.1:p.Glu1233=
|