ENST00000644719.2:c.595T>G
MANE Select
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ENSP00000496625.1:p.Leu199Val
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ENST00000418967.6:c.595T>G
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ENSP00000408860.2:p.Leu199Val
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ENST00000435122.3:c.505T>G
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ENSP00000415043.2:p.Leu169Val
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ENST00000462278.1:n.183T>G
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|
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ENST00000464325.5:n.516T>G
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|
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ENST00000466779.5:c.*287T>G
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ENSP00000417321.1:n.*287T>G
|
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ENST00000466879.5:n.646T>G
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|
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ENST00000469053.5:c.*287T>G
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ENSP00000418104.1:n.*287T>G
|
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ENST00000471671.4:c.556T>G
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ENSP00000418561.1:p.Leu186Val
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ENST00000479074.5:n.653T>G
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|
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ENST00000479730.5:n.711T>G
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|
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ENST00000483041.5:n.764T>G
|
|
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ENST00000486063.5:n.775T>G
|
|
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NM_000500.7:c.595T>G
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NP_000491.4:p.Leu199Val
|
|
NM_001128590.3:c.505T>G
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NP_001122062.3:p.Leu169Val
|
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XM_011514314.1:c.190T>G
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XP_011512616.1:p.Leu64Val
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NM_000500.9:c.595T>G
MANE Select
|
NP_000491.4:p.Leu199Val
|
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NM_001368143.1:c.190T>G
|
NP_001355072.1:p.Leu64Val
|
|
NM_001368144.1:c.190T>G
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NP_001355073.1:p.Leu64Val
|
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NM_001128590.4:c.505T>G
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NP_001122062.3:p.Leu169Val
|
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NM_001368143.2:c.190T>G
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NP_001355072.1:p.Leu64Val
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NM_001368144.2:c.190T>G
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NP_001355073.1:p.Leu64Val
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