ENST00000302850.10:c.3210G>A
MANE Select
|
ENSP00000303830.4:p.Glu1070=
|
|
ENST00000302850.9:c.3210G>A
|
ENSP00000303830.4:p.Glu1070=
|
|
ENST00000341500.9:c.3174G>A
|
ENSP00000342838.4:p.Glu1058=
|
|
ENST00000593970.1:n.56G>A
|
|
|
NM_000208.2:c.3210G>A
|
NP_000199.2:p.Glu1070=
|
|
NM_000208.3:c.3210G>A
|
NP_000199.2:p.Glu1070=
|
|
NM_001079817.1:c.3174G>A
|
NP_001073285.1:p.Glu1058=
|
|
NM_001079817.2:c.3174G>A
|
NP_001073285.1:p.Glu1058=
|
|
XM_011527988.1:c.3285G>A
|
XP_011526290.1:p.Glu1095=
|
|
XM_011527989.1:c.3249G>A
|
XP_011526291.1:p.Glu1083=
|
|
XM_011527988.2:c.3207G>A
|
XP_011526290.2:p.Glu1069=
|
|
XM_011527989.3:c.3171G>A
|
XP_011526291.2:p.Glu1057=
|
|
NM_000208.4:c.3210G>A
MANE Select
|
NP_000199.2:p.Glu1070=
|
|
NM_001079817.3:c.3174G>A
|
NP_001073285.1:p.Glu1058=
|
|