ENST00000644719.2:c.657C>A
MANE Select
|
ENSP00000496625.1:p.Phe219Leu
|
|
ENST00000418967.6:c.657C>A
|
ENSP00000408860.2:p.Phe219Leu
|
|
ENST00000435122.3:c.567C>A
|
ENSP00000415043.2:p.Phe189Leu
|
|
ENST00000462278.1:n.346C>A
|
|
|
ENST00000464325.5:n.578C>A
|
|
|
ENST00000466779.5:c.*349C>A
|
ENSP00000417321.1:n.*349C>A
|
|
ENST00000466879.5:n.708C>A
|
|
|
ENST00000479074.5:n.715C>A
|
|
|
ENST00000479730.5:n.773C>A
|
|
|
ENST00000483041.5:n.826C>A
|
|
|
ENST00000486063.5:n.837C>A
|
|
|
NM_000500.7:c.657C>A
|
NP_000491.4:p.Phe219Leu
|
|
NM_001128590.3:c.567C>A
|
NP_001122062.3:p.Phe189Leu
|
|
XM_011514314.1:c.252C>A
|
XP_011512616.1:p.Phe84Leu
|
|
NM_000500.9:c.657C>A
MANE Select
|
NP_000491.4:p.Phe219Leu
|
|
NM_001368143.1:c.252C>A
|
NP_001355072.1:p.Phe84Leu
|
|
NM_001368144.1:c.252C>A
|
NP_001355073.1:p.Phe84Leu
|
|
NM_001128590.4:c.567C>A
|
NP_001122062.3:p.Phe189Leu
|
|
NM_001368143.2:c.252C>A
|
NP_001355072.1:p.Phe84Leu
|
|
NM_001368144.2:c.252C>A
|
NP_001355073.1:p.Phe84Leu
|
|