ENST00000644719.2:c.1018C>T
MANE Select
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ENSP00000496625.1:p.Arg340Cys
|
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ENST00000418967.6:c.1018C>T
|
ENSP00000408860.2:p.Arg340Cys
|
|
ENST00000435122.3:c.928C>T
|
ENSP00000415043.2:p.Arg310Cys
|
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ENST00000479074.5:n.1076C>T
|
|
|
ENST00000479730.5:n.1134C>T
|
|
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ENST00000483041.5:n.1187C>T
|
|
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ENST00000486063.5:n.997C>T
|
|
|
NM_000500.7:c.1018C>T
|
NP_000491.4:p.Arg340Cys
|
|
NM_001128590.3:c.928C>T
|
NP_001122062.3:p.Arg310Cys
|
|
XM_011514314.1:c.613C>T
|
XP_011512616.1:p.Arg205Cys
|
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NM_000500.9:c.1018C>T
MANE Select
|
NP_000491.4:p.Arg340Cys
|
|
NM_001368143.1:c.613C>T
|
NP_001355072.1:p.Arg205Cys
|
|
NM_001368144.1:c.613C>T
|
NP_001355073.1:p.Arg205Cys
|
|
NM_001128590.4:c.928C>T
|
NP_001122062.3:p.Arg310Cys
|
|
NM_001368143.2:c.613C>T
|
NP_001355072.1:p.Arg205Cys
|
|
NM_001368144.2:c.613C>T
|
NP_001355073.1:p.Arg205Cys
|
|