ENST00000644719.2:c.651G>T
MANE Select
|
ENSP00000496625.1:p.Arg217Ser
|
|
ENST00000418967.6:c.651G>T
|
ENSP00000408860.2:p.Arg217Ser
|
|
ENST00000435122.3:c.561G>T
|
ENSP00000415043.2:p.Arg187Ser
|
|
ENST00000462278.1:n.239G>T
|
|
|
ENST00000464325.5:n.572G>T
|
|
|
ENST00000466779.5:c.*343G>T
|
ENSP00000417321.1:n.*343G>T
|
|
ENST00000466879.5:n.702G>T
|
|
|
ENST00000479074.5:n.709G>T
|
|
|
ENST00000479730.5:n.767G>T
|
|
|
ENST00000483041.5:n.820G>T
|
|
|
ENST00000486063.5:n.831G>T
|
|
|
NM_000500.7:c.651G>T
|
NP_000491.4:p.Arg217Ser
|
|
NM_001128590.3:c.561G>T
|
NP_001122062.3:p.Arg187Ser
|
|
XM_011514314.1:c.246G>T
|
XP_011512616.1:p.Arg82Ser
|
|
NM_000500.9:c.651G>T
MANE Select
|
NP_000491.4:p.Arg217Ser
|
|
NM_001368143.1:c.246G>T
|
NP_001355072.1:p.Arg82Ser
|
|
NM_001368144.1:c.246G>T
|
NP_001355073.1:p.Arg82Ser
|
|
NM_001128590.4:c.561G>T
|
NP_001122062.3:p.Arg187Ser
|
|
NM_001368143.2:c.246G>T
|
NP_001355072.1:p.Arg82Ser
|
|
NM_001368144.2:c.246G>T
|
NP_001355073.1:p.Arg82Ser
|
|