ENST00000456935.7:c.1485G>T
MANE Select
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ENSP00000395473.2:p.Gln495His
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ENST00000221363.8:c.1482G>T
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ENSP00000221363.4:p.Gln494His
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ENST00000433513.5:n.91G>T
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ENST00000456935.6:c.1485G>T
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ENSP00000395473.2:p.Gln495His
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ENST00000466794.5:n.1384G>T
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ENST00000495617.1:n.661G>T
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|
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ENST00000593686.1:c.95G>T
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|
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ENST00000595880.5:n.82G>T
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NM_000528.3:c.1485G>T
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NP_000519.2:p.Gln495His
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NM_001173498.1:c.1482G>T
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NP_001166969.1:p.Gln494His
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XM_005259913.1:c.1488G>T
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XP_005259970.1:p.Gln496His
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XM_011528017.1:c.384G>T
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XP_011526319.1:p.Gln128His
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XM_005259913.2:c.1488G>T
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XP_005259970.1:p.Gln496His
|
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XM_024451518.1:c.384G>T
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XP_024307286.1:p.Gln128His
|
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NM_000528.4:c.1485G>T
MANE Select
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NP_000519.2:p.Gln495His
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NM_001173498.2:c.1482G>T
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NP_001166969.1:p.Gln494His
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