ENST00000644719.2:c.604T>C
MANE Select
|
ENSP00000496625.1:p.Trp202Arg
|
|
ENST00000418967.6:c.604T>C
|
ENSP00000408860.2:p.Trp202Arg
|
|
ENST00000435122.3:c.514T>C
|
ENSP00000415043.2:p.Trp172Arg
|
|
ENST00000462278.1:n.192T>C
|
|
|
ENST00000464325.5:n.525T>C
|
|
|
ENST00000466779.5:c.*296T>C
|
ENSP00000417321.1:n.*296T>C
|
|
ENST00000466879.5:n.655T>C
|
|
|
ENST00000469053.5:c.*296T>C
|
ENSP00000418104.1:n.*296T>C
|
|
ENST00000471671.4:c.565T>C
|
ENSP00000418561.1:p.Trp189Arg
|
|
ENST00000479074.5:n.662T>C
|
|
|
ENST00000479730.5:n.720T>C
|
|
|
ENST00000483041.5:n.773T>C
|
|
|
ENST00000486063.5:n.784T>C
|
|
|
NM_000500.7:c.604T>C
|
NP_000491.4:p.Trp202Arg
|
|
NM_001128590.3:c.514T>C
|
NP_001122062.3:p.Trp172Arg
|
|
XM_011514314.1:c.199T>C
|
XP_011512616.1:p.Trp67Arg
|
|
NM_000500.9:c.604T>C
MANE Select
|
NP_000491.4:p.Trp202Arg
|
|
NM_001368143.1:c.199T>C
|
NP_001355072.1:p.Trp67Arg
|
|
NM_001368144.1:c.199T>C
|
NP_001355073.1:p.Trp67Arg
|
|
NM_001128590.4:c.514T>C
|
NP_001122062.3:p.Trp172Arg
|
|
NM_001368143.2:c.199T>C
|
NP_001355072.1:p.Trp67Arg
|
|
NM_001368144.2:c.199T>C
|
NP_001355073.1:p.Trp67Arg
|
|