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ENSP00000507003.1:n.1812C=
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ENST00000268097.10:c.1481C=
MANE Select
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ENSP00000268097.6:p.Thr494=
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ENST00000268097.9:c.1481C=
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NM_000520.4:c.1481C=
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NP_000511.2:p.Thr494=
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NP_000511.2:p.Thr494=
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NM_001318825.1:c.1514C=
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NP_001305754.1:p.Thr505=
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NR_134869.1:n.1725C=
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NM_000520.6:c.1481C=
MANE Select
|
NP_000511.2:p.Thr494=
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NM_001318825.2:c.1514C=
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NP_001305754.1:p.Thr505=
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NR_134869.2:n.1266C=
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NR_134869.3:n.1266C=
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