ENST00000644719.2:c.387G>T
MANE Select
|
ENSP00000496625.1:p.Leu129=
|
|
ENST00000418967.6:c.387G>T
|
ENSP00000408860.2:p.Leu129=
|
|
ENST00000435122.3:c.297G>T
|
ENSP00000415043.2:p.Leu99=
|
|
ENST00000464325.5:n.308G>T
|
|
|
ENST00000466779.5:c.*79G>T
|
ENSP00000417321.1:n.*79G>T
|
|
ENST00000466879.5:n.438G>T
|
|
|
ENST00000469053.5:c.*79G>T
|
ENSP00000418104.1:n.*79G>T
|
|
ENST00000471671.4:c.387G>T
|
ENSP00000418561.1:p.Leu129=
|
|
ENST00000478281.5:c.420G>T
|
ENSP00000419572.1:p.Leu140=
|
|
ENST00000479074.5:n.445G>T
|
|
|
ENST00000479730.5:n.542G>T
|
|
|
ENST00000483041.5:n.556G>T
|
|
|
ENST00000486063.5:n.567G>T
|
|
|
ENST00000488465.1:n.395G>T
|
|
|
NM_000500.7:c.387G>T
|
NP_000491.4:p.Leu129=
|
|
NM_001128590.3:c.297G>T
|
NP_001122062.3:p.Leu99=
|
|
XM_011514314.1:c.-19G>T
|
XP_011512616.1:n.-19G>T
|
|
NM_000500.9:c.387G>T
MANE Select
|
NP_000491.4:p.Leu129=
|
|
NM_001368143.1:c.-19G>T
|
NP_001355072.1:n.-19G>T
|
|
NM_001368144.1:c.-19G>T
|
NP_001355073.1:n.-19G>T
|
|
NM_001128590.4:c.297G>T
|
NP_001122062.3:p.Leu99=
|
|
NM_001368143.2:c.-19G>T
|
NP_001355072.1:n.-19G>T
|
|
NM_001368144.2:c.-19G>T
|
NP_001355073.1:n.-19G>T
|
|