ENST00000696170.1:c.*23A>G
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ENSP00000512461.1:n.*23A>G
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ENST00000696171.1:c.418A>G
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ENSP00000512462.1:p.Thr140Ala
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ENST00000696172.1:c.338-2974A>G
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ENSP00000512463.1:n.338-2974A>G
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ENST00000378588.5:c.514A>G
MANE Select
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ENSP00000367851.4:p.Thr172Ala
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ENST00000378588.4:c.514A>G
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ENSP00000367851.4:p.Thr172Ala
|
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ENST00000465127.1:c.171+369981A>G
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ENSP00000417050.1:n.171+369981A>G
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NM_000397.3:c.514A>G , LRG_53t1:c.514A>G
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NP_000388.2:p.Thr172Ala
|
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XM_011543890.1:c.208A>G
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XP_011542192.1:p.Thr70Ala
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NM_000397.4:c.514A>G
MANE Select
|
NP_000388.2:p.Thr172Ala
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|