ENST00000644719.2:c.653T>A
MANE Select
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ENSP00000496625.1:p.Phe218Tyr
|
|
ENST00000418967.6:c.653T>A
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ENSP00000408860.2:p.Phe218Tyr
|
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ENST00000435122.3:c.563T>A
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ENSP00000415043.2:p.Phe188Tyr
|
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ENST00000462278.1:n.342T>A
|
|
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ENST00000464325.5:n.574T>A
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|
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ENST00000466779.5:c.*345T>A
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ENSP00000417321.1:n.*345T>A
|
|
ENST00000466879.5:n.704T>A
|
|
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ENST00000479074.5:n.711T>A
|
|
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ENST00000479730.5:n.769T>A
|
|
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ENST00000483041.5:n.822T>A
|
|
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ENST00000486063.5:n.833T>A
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|
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NM_000500.7:c.653T>A
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NP_000491.4:p.Phe218Tyr
|
|
NM_001128590.3:c.563T>A
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NP_001122062.3:p.Phe188Tyr
|
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XM_011514314.1:c.248T>A
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XP_011512616.1:p.Phe83Tyr
|
|
NM_000500.9:c.653T>A
MANE Select
|
NP_000491.4:p.Phe218Tyr
|
|
NM_001368143.1:c.248T>A
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NP_001355072.1:p.Phe83Tyr
|
|
NM_001368144.1:c.248T>A
|
NP_001355073.1:p.Phe83Tyr
|
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NM_001128590.4:c.563T>A
|
NP_001122062.3:p.Phe188Tyr
|
|
NM_001368143.2:c.248T>A
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NP_001355072.1:p.Phe83Tyr
|
|
NM_001368144.2:c.248T>A
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NP_001355073.1:p.Phe83Tyr
|
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