ENST00000302850.10:c.3854A>T
MANE Select
|
ENSP00000303830.4:p.Glu1285Val
|
|
ENST00000302850.9:c.3854A>T
|
ENSP00000303830.4:p.Glu1285Val
|
|
ENST00000341500.9:c.3818A>T
|
ENSP00000342838.4:p.Glu1273Val
|
|
NM_000208.2:c.3854A>T
|
NP_000199.2:p.Glu1285Val
|
|
NM_000208.3:c.3854A>T
|
NP_000199.2:p.Glu1285Val
|
|
NM_001079817.1:c.3818A>T
|
NP_001073285.1:p.Glu1273Val
|
|
NM_001079817.2:c.3818A>T
|
NP_001073285.1:p.Glu1273Val
|
|
XM_011527988.1:c.3929A>T
|
XP_011526290.1:p.Glu1310Val
|
|
XM_011527989.1:c.3893A>T
|
XP_011526291.1:p.Glu1298Val
|
|
XM_011527988.2:c.3851A>T
|
XP_011526290.2:p.Glu1284Val
|
|
XM_011527989.3:c.3815A>T
|
XP_011526291.2:p.Glu1272Val
|
|
NM_000208.4:c.3854A>T
MANE Select
|
NP_000199.2:p.Glu1285Val
|
|
NM_001079817.3:c.3818A>T
|
NP_001073285.1:p.Glu1273Val
|
|