ENST00000644719.2:c.436G>A
MANE Select
|
ENSP00000496625.1:p.Glu146Lys
|
|
ENST00000418967.6:c.436G>A
|
ENSP00000408860.2:p.Glu146Lys
|
|
ENST00000435122.3:c.346G>A
|
ENSP00000415043.2:p.Glu116Lys
|
|
ENST00000462278.1:n.24G>A
|
|
|
ENST00000464325.5:n.357G>A
|
|
|
ENST00000466779.5:c.*128G>A
|
ENSP00000417321.1:n.*128G>A
|
|
ENST00000466879.5:n.487G>A
|
|
|
ENST00000469053.5:c.*128G>A
|
ENSP00000418104.1:n.*128G>A
|
|
ENST00000471671.4:c.436G>A
|
ENSP00000418561.1:p.Glu146Lys
|
|
ENST00000478281.5:c.469G>A
|
ENSP00000419572.1:p.Glu157Lys
|
|
ENST00000479074.5:n.494G>A
|
|
|
ENST00000479730.5:n.591G>A
|
|
|
ENST00000483041.5:n.605G>A
|
|
|
ENST00000486063.5:n.616G>A
|
|
|
ENST00000488465.1:n.444G>A
|
|
|
NM_000500.7:c.436G>A
|
NP_000491.4:p.Glu146Lys
|
|
NM_001128590.3:c.346G>A
|
NP_001122062.3:p.Glu116Lys
|
|
XM_011514314.1:c.31G>A
|
XP_011512616.1:p.Glu11Lys
|
|
NM_000500.9:c.436G>A
MANE Select
|
NP_000491.4:p.Glu146Lys
|
|
NM_001368143.1:c.31G>A
|
NP_001355072.1:p.Glu11Lys
|
|
NM_001368144.1:c.31G>A
|
NP_001355073.1:p.Glu11Lys
|
|
NM_001128590.4:c.346G>A
|
NP_001122062.3:p.Glu116Lys
|
|
NM_001368143.2:c.31G>A
|
NP_001355072.1:p.Glu11Lys
|
|
NM_001368144.2:c.31G>A
|
NP_001355073.1:p.Glu11Lys
|
|