ENST00000644719.2:c.444T>A
MANE Select
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ENSP00000496625.1:p.Cys148Ter
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ENST00000418967.6:c.444T>A
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ENSP00000408860.2:p.Cys148Ter
|
|
ENST00000435122.3:c.354T>A
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ENSP00000415043.2:p.Cys118Ter
|
|
ENST00000462278.1:n.32T>A
|
|
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ENST00000464325.5:n.365T>A
|
|
|
ENST00000466779.5:c.*136T>A
|
ENSP00000417321.1:n.*136T>A
|
|
ENST00000466879.5:n.495T>A
|
|
|
ENST00000469053.5:c.*136T>A
|
ENSP00000418104.1:n.*136T>A
|
|
ENST00000471671.4:c.444T>A
|
ENSP00000418561.1:p.Cys148Ter
|
|
ENST00000478281.5:c.477T>A
|
ENSP00000419572.1:p.Cys159Ter
|
|
ENST00000479074.5:n.502T>A
|
|
|
ENST00000479730.5:n.599T>A
|
|
|
ENST00000483041.5:n.613T>A
|
|
|
ENST00000486063.5:n.624T>A
|
|
|
ENST00000488465.1:n.452T>A
|
|
|
NM_000500.7:c.444T>A
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NP_000491.4:p.Cys148Ter
|
|
NM_001128590.3:c.354T>A
|
NP_001122062.3:p.Cys118Ter
|
|
XM_011514314.1:c.39T>A
|
XP_011512616.1:p.Cys13Ter
|
|
NM_000500.9:c.444T>A
MANE Select
|
NP_000491.4:p.Cys148Ter
|
|
NM_001368143.1:c.39T>A
|
NP_001355072.1:p.Cys13Ter
|
|
NM_001368144.1:c.39T>A
|
NP_001355073.1:p.Cys13Ter
|
|
NM_001128590.4:c.354T>A
|
NP_001122062.3:p.Cys118Ter
|
|
NM_001368143.2:c.39T>A
|
NP_001355072.1:p.Cys13Ter
|
|
NM_001368144.2:c.39T>A
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NP_001355073.1:p.Cys13Ter
|
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