ENST00000302850.10:c.3945G>A
MANE Select
|
ENSP00000303830.4:p.Glu1315=
|
|
ENST00000302850.9:c.3945G>A
|
ENSP00000303830.4:p.Glu1315=
|
|
ENST00000341500.9:c.3909G>A
|
ENSP00000342838.4:p.Glu1303=
|
|
NM_000208.2:c.3945G>A
|
NP_000199.2:p.Glu1315=
|
|
NM_000208.3:c.3945G>A
|
NP_000199.2:p.Glu1315=
|
|
NM_001079817.1:c.3909G>A
|
NP_001073285.1:p.Glu1303=
|
|
NM_001079817.2:c.3909G>A
|
NP_001073285.1:p.Glu1303=
|
|
XM_011527988.1:c.4020G>A
|
XP_011526290.1:p.Glu1340=
|
|
XM_011527989.1:c.3984G>A
|
XP_011526291.1:p.Glu1328=
|
|
XM_011527988.2:c.3942G>A
|
XP_011526290.2:p.Glu1314=
|
|
XM_011527989.3:c.3906G>A
|
XP_011526291.2:p.Glu1302=
|
|
NM_000208.4:c.3945G>A
MANE Select
|
NP_000199.2:p.Glu1315=
|
|
NM_001079817.3:c.3909G>A
|
NP_001073285.1:p.Glu1303=
|
|