ENST00000425340.3:c.663_667delinsATACC
MANE Select
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ENSP00000387498.2:p.Arg221=
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ENST00000522966.2:c.663_667delinsATACC
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ENSP00000430227.2:p.Arg221=
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ENST00000391876.5:c.663_667delinsATACC
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ENSP00000375748.4:p.Arg221=
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ENST00000425340.2:c.663_667delinsATACC
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ENSP00000387498.2:p.Arg221=
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NM_000511.5:c.663_667delinsATACC
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NP_000502.4:p.Arg221=
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NM_001097638.2:c.663_667delinsATACC
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NP_001091107.1:p.Arg221=
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NR_131188.1:n.226_230delinsGGTAT
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NM_000511.6:c.663_667delinsATACC
MANE Select
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NP_000502.4:p.Arg221=
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NM_001097638.3:c.663_667delinsATACC
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NP_001091107.1:p.Arg221=
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