ENST00000644719.2:c.300G=
MANE Select
|
ENSP00000496625.1:p.Leu100=
|
|
ENST00000418967.6:c.300G=
|
ENSP00000408860.2:p.Leu100=
|
|
ENST00000435122.3:c.210G=
|
ENSP00000415043.2:p.Leu70=
|
|
ENST00000464325.5:n.230-9G=
|
|
|
ENST00000466779.5:c.319G=
|
ENSP00000417321.1:p.Gly107=
|
|
ENST00000466879.5:n.351G=
|
|
|
ENST00000469053.5:c.229G=
|
ENSP00000418104.1:p.Gly77=
|
|
ENST00000471671.4:c.300G=
|
ENSP00000418561.1:p.Leu100=
|
|
ENST00000478281.5:c.333G=
|
ENSP00000419572.1:p.Leu111=
|
|
ENST00000479074.5:n.358G=
|
|
|
ENST00000479730.5:n.455G=
|
|
|
ENST00000480027.1:n.635G=
|
|
|
ENST00000483041.5:n.469G=
|
|
|
ENST00000486063.5:n.480G=
|
|
|
ENST00000488465.1:n.308G=
|
|
|
NM_000500.7:c.300G=
|
NP_000491.4:p.Leu100=
|
|
NM_001128590.3:c.210G=
|
NP_001122062.3:p.Leu70=
|
|
XM_011514314.1:c.-106G=
|
XP_011512616.1:n.-106G=
|
|
NM_000500.9:c.300G=
MANE Select
|
NP_000491.4:p.Leu100=
|
|
NM_001368143.1:c.-106G=
|
NP_001355072.1:n.-106G=
|
|
NM_001368144.1:c.-106G=
|
NP_001355073.1:n.-106G=
|
|
NM_001128590.4:c.210G=
|
NP_001122062.3:p.Leu70=
|
|
NM_001368143.2:c.-106G=
|
NP_001355072.1:n.-106G=
|
|
NM_001368144.2:c.-106G=
|
NP_001355073.1:n.-106G=
|
|