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NM_000520.6:c.637T=
MANE Select
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NP_000511.2:p.Tyr213=
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ENST00000268097.10:c.637T=
MANE Select
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ENSP00000268097.6:p.Tyr213=
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NM_000520.4:c.637T=
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NP_000511.2:p.Tyr213=
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NP_000511.2:p.Tyr213=
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NM_001318825.2:c.670T=
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NP_001305754.1:p.Tyr224=
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|
|
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ENST00000684667.1:c.968T=
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ENSP00000507003.1:n.968T=
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