ENST00000321612.8:c.2087T>C
MANE Select
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ENSP00000370737.4:p.Met696Thr
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ENST00000638233.1:n.522T>C
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|
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ENST00000638661.1:c.287T>C
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ENSP00000491369.1:p.Met96Thr
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ENST00000638694.1:n.274T>C
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|
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ENST00000639318.1:c.287T>C
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ENSP00000491932.1:p.Met96Thr
|
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ENST00000639364.1:n.1787T>C
|
|
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ENST00000639443.1:n.1655T>C
|
|
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ENST00000639954.1:n.1795T>C
|
|
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ENST00000640505.1:n.326T>C
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|
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ENST00000321612.6:c.2087T>C
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ENSP00000370737.3:p.Met696Thr
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NM_000170.2:c.2087T>C , LRG_643t1:c.2087T>C
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NP_000161.2:p.Met696Thr
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NM_000170.3:c.2087T>C
MANE Select
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NP_000161.2:p.Met696Thr
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