ENST00000376228.10:c.991_992insCTG
MANE Select
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ENSP00000365402.5:p.Met331delinsThrVal
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ENST00000376228.9:c.991_992insCTG
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ENSP00000365402.5:p.Met331delinsThrVal
|
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ENST00000376237.8:c.*578_*579insCTG
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ENSP00000365412.4:n.*578_*579insCTG
|
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ENST00000383329.7:c.991_992insCTG
|
ENSP00000372819.3:p.Met331delinsThrVal
|
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ENST00000470363.5:n.309_310insCTG
|
|
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ENST00000487245.5:n.1350_1351insCTG
|
|
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NM_002117.5:c.991_992insCTG
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NP_002108.4:p.Met331delinsThrVal
|
|
NM_002117.6:c.991_992insCTG
MANE Select
|
NP_002108.4:p.Met331delinsThrVal
|
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