ENST00000644719.2:c.644T>C
MANE Select
|
ENSP00000496625.1:p.Phe215Ser
|
|
ENST00000418967.6:c.644T>C
|
ENSP00000408860.2:p.Phe215Ser
|
|
ENST00000435122.3:c.554T>C
|
ENSP00000415043.2:p.Phe185Ser
|
|
ENST00000462278.1:n.232T>C
|
|
|
ENST00000464325.5:n.565T>C
|
|
|
ENST00000466779.5:c.*336T>C
|
ENSP00000417321.1:n.*336T>C
|
|
ENST00000466879.5:n.695T>C
|
|
|
ENST00000469053.5:c.*336T>C
|
ENSP00000418104.1:n.*336T>C
|
|
ENST00000479074.5:n.702T>C
|
|
|
ENST00000479730.5:n.760T>C
|
|
|
ENST00000483041.5:n.813T>C
|
|
|
ENST00000486063.5:n.824T>C
|
|
|
NM_000500.7:c.644T>C
|
NP_000491.4:p.Phe215Ser
|
|
NM_001128590.3:c.554T>C
|
NP_001122062.3:p.Phe185Ser
|
|
XM_011514314.1:c.239T>C
|
XP_011512616.1:p.Phe80Ser
|
|
NM_000500.9:c.644T>C
MANE Select
|
NP_000491.4:p.Phe215Ser
|
|
NM_001368143.1:c.239T>C
|
NP_001355072.1:p.Phe80Ser
|
|
NM_001368144.1:c.239T>C
|
NP_001355073.1:p.Phe80Ser
|
|
NM_001128590.4:c.554T>C
|
NP_001122062.3:p.Phe185Ser
|
|
NM_001368143.2:c.239T>C
|
NP_001355072.1:p.Phe80Ser
|
|
NM_001368144.2:c.239T>C
|
NP_001355073.1:p.Phe80Ser
|
|