ENST00000559133.6:c.6925A>G
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ENSP00000453958.2:p.Asn2309Asp
|
|
ENST00000674301.2:c.*376A>G
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ENSP00000501333.2:n.*376A>G
|
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ENST00000682170.1:n.534A>G
|
|
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ENST00000682767.1:n.160A>G
|
|
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ENST00000316623.10:c.6925A>G
MANE Select
|
ENSP00000325527.5:p.Asn2309Asp
|
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ENST00000674301.1:c.2029A>G
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ENSP00000501333.1:n.2029A>G
|
|
ENST00000316623.9:c.6925A>G
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ENSP00000325527.5:p.Asn2309Asp
|
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ENST00000559133.5:c.2232A>G
|
|
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ENST00000560720.1:n.212A>G
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|
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NM_000138.4:c.6925A>G , LRG_778t1:c.6925A>G
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NP_000129.3:p.Asn2309Asp
|
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NM_000138.5:c.6925A>G
MANE Select
|
NP_000129.3:p.Asn2309Asp
|
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