ENST00000315757.9:c.1328C>G
MANE Select
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ENSP00000327290.7:p.Ala443Gly
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ENST00000315757.8:c.1328C>G
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ENSP00000327290.7:p.Ala443Gly
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ENST00000423218.6:c.1328C>G
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ENSP00000403392.2:p.Ala443Gly
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ENST00000566429.1:n.217C>G
|
|
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ENST00000569346.5:n.307C>G
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NM_001004439.1:c.1328C>G
|
NP_001004439.1:p.Ala443Gly
|
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XM_005254228.2:c.1022C>G
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XP_005254285.1:p.Ala341Gly
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XM_011521363.1:c.1121C>G
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XP_011519665.1:p.Ala374Gly
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XM_005254228.3:c.1022C>G
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XP_005254285.1:p.Ala341Gly
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XM_011521363.2:c.1121C>G
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XP_011519665.1:p.Ala374Gly
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NM_001004439.2:c.1328C>G
MANE Select
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NP_001004439.1:p.Ala443Gly
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