ENST00000302850.10:c.4017G>A
MANE Select
|
ENSP00000303830.4:p.Glu1339=
|
|
ENST00000302850.9:c.4017G>A
|
ENSP00000303830.4:p.Glu1339=
|
|
ENST00000341500.9:c.3981G>A
|
ENSP00000342838.4:p.Glu1327=
|
|
NM_000208.2:c.4017G>A
|
NP_000199.2:p.Glu1339=
|
|
NM_000208.3:c.4017G>A
|
NP_000199.2:p.Glu1339=
|
|
NM_001079817.1:c.3981G>A
|
NP_001073285.1:p.Glu1327=
|
|
NM_001079817.2:c.3981G>A
|
NP_001073285.1:p.Glu1327=
|
|
XM_011527988.1:c.4092G>A
|
XP_011526290.1:p.Glu1364=
|
|
XM_011527989.1:c.4056G>A
|
XP_011526291.1:p.Glu1352=
|
|
XM_011527988.2:c.4014G>A
|
XP_011526290.2:p.Glu1338=
|
|
XM_011527989.3:c.3978G>A
|
XP_011526291.2:p.Glu1326=
|
|
NM_000208.4:c.4017G>A
MANE Select
|
NP_000199.2:p.Glu1339=
|
|
NM_001079817.3:c.3981G>A
|
NP_001073285.1:p.Glu1327=
|
|