ENST00000559133.6:c.*804A>G
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ENSP00000453958.2:n.*804A>G
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ENST00000674301.2:c.*1509A>G
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ENSP00000501333.2:n.*1509A>G
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ENST00000682158.1:n.1377A>G
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ENST00000682170.1:n.2177A>G
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|
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ENST00000682767.1:n.1293A>G
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ENST00000316623.10:c.7996A>G
MANE Select
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ENSP00000325527.5:p.Thr2666Ala
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ENST00000674301.1:c.3162A>G
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ENSP00000501333.1:n.3162A>G
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ENST00000316623.9:c.7996A>G
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ENSP00000325527.5:p.Thr2666Ala
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ENST00000559133.5:c.3365A>G
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|
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ENST00000561429.1:n.251A>G
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|
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NM_000138.4:c.7996A>G , LRG_778t1:c.7996A>G
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NP_000129.3:p.Thr2666Ala
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NM_000138.5:c.7996A>G
MANE Select
|
NP_000129.3:p.Thr2666Ala
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