ENST00000302850.10:c.4016A>T
MANE Select
|
ENSP00000303830.4:p.Glu1339Val
|
|
ENST00000302850.9:c.4016A>T
|
ENSP00000303830.4:p.Glu1339Val
|
|
ENST00000341500.9:c.3980A>T
|
ENSP00000342838.4:p.Glu1327Val
|
|
NM_000208.2:c.4016A>T
|
NP_000199.2:p.Glu1339Val
|
|
NM_000208.3:c.4016A>T
|
NP_000199.2:p.Glu1339Val
|
|
NM_001079817.1:c.3980A>T
|
NP_001073285.1:p.Glu1327Val
|
|
NM_001079817.2:c.3980A>T
|
NP_001073285.1:p.Glu1327Val
|
|
XM_011527988.1:c.4091A>T
|
XP_011526290.1:p.Glu1364Val
|
|
XM_011527989.1:c.4055A>T
|
XP_011526291.1:p.Glu1352Val
|
|
XM_011527988.2:c.4013A>T
|
XP_011526290.2:p.Glu1338Val
|
|
XM_011527989.3:c.3977A>T
|
XP_011526291.2:p.Glu1326Val
|
|
NM_000208.4:c.4016A>T
MANE Select
|
NP_000199.2:p.Glu1339Val
|
|
NM_001079817.3:c.3980A>T
|
NP_001073285.1:p.Glu1327Val
|
|