ENST00000302850.10:c.3974A>T
MANE Select
|
ENSP00000303830.4:p.Glu1325Val
|
|
ENST00000302850.9:c.3974A>T
|
ENSP00000303830.4:p.Glu1325Val
|
|
ENST00000341500.9:c.3938A>T
|
ENSP00000342838.4:p.Glu1313Val
|
|
NM_000208.2:c.3974A>T
|
NP_000199.2:p.Glu1325Val
|
|
NM_000208.3:c.3974A>T
|
NP_000199.2:p.Glu1325Val
|
|
NM_001079817.1:c.3938A>T
|
NP_001073285.1:p.Glu1313Val
|
|
NM_001079817.2:c.3938A>T
|
NP_001073285.1:p.Glu1313Val
|
|
XM_011527988.1:c.4049A>T
|
XP_011526290.1:p.Glu1350Val
|
|
XM_011527989.1:c.4013A>T
|
XP_011526291.1:p.Glu1338Val
|
|
XM_011527988.2:c.3971A>T
|
XP_011526290.2:p.Glu1324Val
|
|
XM_011527989.3:c.3935A>T
|
XP_011526291.2:p.Glu1312Val
|
|
NM_000208.4:c.3974A>T
MANE Select
|
NP_000199.2:p.Glu1325Val
|
|
NM_001079817.3:c.3938A>T
|
NP_001073285.1:p.Glu1313Val
|
|