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ENST00000684667.1:c.1495C=
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ENSP00000507003.1:n.1495C=
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ENST00000268097.10:c.1164C=
MANE Select
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ENSP00000268097.6:p.Ile388=
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ENST00000268097.9:c.1164C=
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ENSP00000268097.5:p.Ile388=
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NP_000511.2:p.Ile388=
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NP_000511.2:p.Ile388=
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NP_001305754.1:p.Ile399=
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NR_134869.1:n.1575-368C=
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NM_000520.6:c.1164C=
MANE Select
|
NP_000511.2:p.Ile388=
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NM_001318825.2:c.1197C=
|
NP_001305754.1:p.Ile399=
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NR_134869.2:n.1116-368C=
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NR_134869.3:n.1116-368C=
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