ENST00000644719.2:c.532T>A
MANE Select
|
ENSP00000496625.1:p.Phe178Ile
|
|
ENST00000418967.6:c.532T>A
|
ENSP00000408860.2:p.Phe178Ile
|
|
ENST00000435122.3:c.442T>A
|
ENSP00000415043.2:p.Phe148Ile
|
|
ENST00000462278.1:n.120T>A
|
|
|
ENST00000464325.5:n.453T>A
|
|
|
ENST00000466779.5:c.*224T>A
|
ENSP00000417321.1:n.*224T>A
|
|
ENST00000466879.5:n.583T>A
|
|
|
ENST00000469053.5:c.*224T>A
|
ENSP00000418104.1:n.*224T>A
|
|
ENST00000471671.4:c.532T>A
|
ENSP00000418561.1:p.Phe178Ile
|
|
ENST00000479074.5:n.590T>A
|
|
|
ENST00000479730.5:n.687T>A
|
|
|
ENST00000483041.5:n.701T>A
|
|
|
ENST00000486063.5:n.712T>A
|
|
|
ENST00000488465.1:n.540T>A
|
|
|
NM_000500.7:c.532T>A
|
NP_000491.4:p.Phe178Ile
|
|
NM_001128590.3:c.442T>A
|
NP_001122062.3:p.Phe148Ile
|
|
XM_011514314.1:c.127T>A
|
XP_011512616.1:p.Phe43Ile
|
|
NM_000500.9:c.532T>A
MANE Select
|
NP_000491.4:p.Phe178Ile
|
|
NM_001368143.1:c.127T>A
|
NP_001355072.1:p.Phe43Ile
|
|
NM_001368144.1:c.127T>A
|
NP_001355073.1:p.Phe43Ile
|
|
NM_001128590.4:c.442T>A
|
NP_001122062.3:p.Phe148Ile
|
|
NM_001368143.2:c.127T>A
|
NP_001355072.1:p.Phe43Ile
|
|
NM_001368144.2:c.127T>A
|
NP_001355073.1:p.Phe43Ile
|
|