ENST00000644719.2:c.621C>T
MANE Select
|
ENSP00000496625.1:p.Ile207=
|
|
ENST00000418967.6:c.621C>T
|
ENSP00000408860.2:p.Ile207=
|
|
ENST00000435122.3:c.531C>T
|
ENSP00000415043.2:p.Ile177=
|
|
ENST00000462278.1:n.209C>T
|
|
|
ENST00000464325.5:n.542C>T
|
|
|
ENST00000466779.5:c.*313C>T
|
ENSP00000417321.1:n.*313C>T
|
|
ENST00000466879.5:n.672C>T
|
|
|
ENST00000469053.5:c.*313C>T
|
ENSP00000418104.1:n.*313C>T
|
|
ENST00000479074.5:n.679C>T
|
|
|
ENST00000479730.5:n.737C>T
|
|
|
ENST00000483041.5:n.790C>T
|
|
|
ENST00000486063.5:n.801C>T
|
|
|
NM_000500.7:c.621C>T
|
NP_000491.4:p.Ile207=
|
|
NM_001128590.3:c.531C>T
|
NP_001122062.3:p.Ile177=
|
|
XM_011514314.1:c.216C>T
|
XP_011512616.1:p.Ile72=
|
|
NM_000500.9:c.621C>T
MANE Select
|
NP_000491.4:p.Ile207=
|
|
NM_001368143.1:c.216C>T
|
NP_001355072.1:p.Ile72=
|
|
NM_001368144.1:c.216C>T
|
NP_001355073.1:p.Ile72=
|
|
NM_001128590.4:c.531C>T
|
NP_001122062.3:p.Ile177=
|
|
NM_001368143.2:c.216C>T
|
NP_001355072.1:p.Ile72=
|
|
NM_001368144.2:c.216C>T
|
NP_001355073.1:p.Ile72=
|
|