ENST00000644719.2:c.1204C>G
MANE Select
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ENSP00000496625.1:p.Pro402Ala
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ENST00000418967.6:c.1204C>G
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ENSP00000408860.2:p.Pro402Ala
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ENST00000435122.3:c.1114C>G
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ENSP00000415043.2:p.Pro372Ala
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ENST00000479074.5:n.1345C>G
|
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ENST00000479730.5:n.1320C>G
|
|
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ENST00000483041.5:n.1373C>G
|
|
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ENST00000486063.5:n.1183C>G
|
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NM_000500.7:c.1204C>G
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NP_000491.4:p.Pro402Ala
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NM_001128590.3:c.1114C>G
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NP_001122062.3:p.Pro372Ala
|
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XM_011514314.1:c.799C>G
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XP_011512616.1:p.Pro267Ala
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NM_000500.9:c.1204C>G
MANE Select
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NP_000491.4:p.Pro402Ala
|
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NM_001368143.1:c.799C>G
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NP_001355072.1:p.Pro267Ala
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NM_001368144.1:c.799C>G
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NP_001355073.1:p.Pro267Ala
|
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NM_001128590.4:c.1114C>G
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NP_001122062.3:p.Pro372Ala
|
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NM_001368143.2:c.799C>G
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NP_001355072.1:p.Pro267Ala
|
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NM_001368144.2:c.799C>G
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NP_001355073.1:p.Pro267Ala
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