ENST00000321612.8:c.2062C>A
MANE Select
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ENSP00000370737.4:p.His688Asn
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ENST00000638233.1:n.497C>A
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|
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ENST00000638661.1:c.262C>A
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ENSP00000491369.1:p.His88Asn
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ENST00000638694.1:n.249C>A
|
|
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ENST00000639318.1:c.262C>A
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ENSP00000491932.1:p.His88Asn
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|
ENST00000639364.1:n.1762C>A
|
|
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ENST00000639443.1:n.1630C>A
|
|
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ENST00000639954.1:n.1770C>A
|
|
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ENST00000640505.1:n.301C>A
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|
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ENST00000321612.6:c.2062C>A
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ENSP00000370737.3:p.His688Asn
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NM_000170.2:c.2062C>A , LRG_643t1:c.2062C>A
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NP_000161.2:p.His688Asn
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NM_000170.3:c.2062C>A
MANE Select
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NP_000161.2:p.His688Asn
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