ENST00000456935.7:c.1480C>G
MANE Select
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ENSP00000395473.2:p.Gln494Glu
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ENST00000221363.8:c.1477C>G
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ENSP00000221363.4:p.Gln493Glu
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ENST00000433513.5:n.86C>G
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ENST00000456935.6:c.1480C>G
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ENSP00000395473.2:p.Gln494Glu
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ENST00000466794.5:n.1379C>G
|
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ENST00000495617.1:n.656C>G
|
|
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ENST00000593686.1:c.90C>G
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|
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ENST00000595880.5:n.77C>G
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|
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NM_000528.3:c.1480C>G
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NP_000519.2:p.Gln494Glu
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NM_001173498.1:c.1477C>G
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NP_001166969.1:p.Gln493Glu
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XM_005259913.1:c.1483C>G
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XP_005259970.1:p.Gln495Glu
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XM_011528017.1:c.379C>G
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XP_011526319.1:p.Gln127Glu
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XM_005259913.2:c.1483C>G
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XP_005259970.1:p.Gln495Glu
|
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XM_024451518.1:c.379C>G
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XP_024307286.1:p.Gln127Glu
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NM_000528.4:c.1480C>G
MANE Select
|
NP_000519.2:p.Gln494Glu
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NM_001173498.2:c.1477C>G
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NP_001166969.1:p.Gln493Glu
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