ENST00000302850.10:c.3182A>T
MANE Select
|
ENSP00000303830.4:p.Glu1061Val
|
|
ENST00000302850.9:c.3182A>T
|
ENSP00000303830.4:p.Glu1061Val
|
|
ENST00000341500.9:c.3146A>T
|
ENSP00000342838.4:p.Glu1049Val
|
|
ENST00000593970.1:n.28A>T
|
|
|
NM_000208.2:c.3182A>T
|
NP_000199.2:p.Glu1061Val
|
|
NM_000208.3:c.3182A>T
|
NP_000199.2:p.Glu1061Val
|
|
NM_001079817.1:c.3146A>T
|
NP_001073285.1:p.Glu1049Val
|
|
NM_001079817.2:c.3146A>T
|
NP_001073285.1:p.Glu1049Val
|
|
XM_011527988.1:c.3257A>T
|
XP_011526290.1:p.Glu1086Val
|
|
XM_011527989.1:c.3221A>T
|
XP_011526291.1:p.Glu1074Val
|
|
XM_011527988.2:c.3179A>T
|
XP_011526290.2:p.Glu1060Val
|
|
XM_011527989.3:c.3143A>T
|
XP_011526291.2:p.Glu1048Val
|
|
NM_000208.4:c.3182A>T
MANE Select
|
NP_000199.2:p.Glu1061Val
|
|
NM_001079817.3:c.3146A>T
|
NP_001073285.1:p.Glu1049Val
|
|