ENST00000644719.2:c.654C>T
MANE Select
|
ENSP00000496625.1:p.Phe218=
|
|
ENST00000418967.6:c.654C>T
|
ENSP00000408860.2:p.Phe218=
|
|
ENST00000435122.3:c.564C>T
|
ENSP00000415043.2:p.Phe188=
|
|
ENST00000462278.1:n.343C>T
|
|
|
ENST00000464325.5:n.575C>T
|
|
|
ENST00000466779.5:c.*346C>T
|
ENSP00000417321.1:n.*346C>T
|
|
ENST00000466879.5:n.705C>T
|
|
|
ENST00000479074.5:n.712C>T
|
|
|
ENST00000479730.5:n.770C>T
|
|
|
ENST00000483041.5:n.823C>T
|
|
|
ENST00000486063.5:n.834C>T
|
|
|
NM_000500.7:c.654C>T
|
NP_000491.4:p.Phe218=
|
|
NM_001128590.3:c.564C>T
|
NP_001122062.3:p.Phe188=
|
|
XM_011514314.1:c.249C>T
|
XP_011512616.1:p.Phe83=
|
|
NM_000500.9:c.654C>T
MANE Select
|
NP_000491.4:p.Phe218=
|
|
NM_001368143.1:c.249C>T
|
NP_001355072.1:p.Phe83=
|
|
NM_001368144.1:c.249C>T
|
NP_001355073.1:p.Phe83=
|
|
NM_001128590.4:c.564C>T
|
NP_001122062.3:p.Phe188=
|
|
NM_001368143.2:c.249C>T
|
NP_001355072.1:p.Phe83=
|
|
NM_001368144.2:c.249C>T
|
NP_001355073.1:p.Phe83=
|
|