ENST00000369085.8:c.779_794delinsTGCGGGCGGCATCCCC
MANE Select
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ENSP00000358081.4:p.Leu260=
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ENST00000369085.7:c.779_794delinsTGCGGGCGGCATCCCC
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ENSP00000358081.3:p.Leu260=
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ENST00000450186.1:c.605_620delinsTGCGGGCGGCATCCCC
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ENSP00000410036.1:p.Leu202=
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NM_004281.3:c.779_794delinsTGCGGGCGGCATCCCC , LRG_742t1:c.779_794delinsTGCGGGCGGCATCCCC
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NP_004272.2:p.Leu260=
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XM_005270287.1:c.779_794delinsTGCGGGCGGCATCCCC
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XP_005270344.1:p.Leu260=
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XM_005270287.2:c.779_794delinsTGCGGGCGGCATCCCC
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XP_005270344.1:p.Leu260=
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NM_004281.4:c.779_794delinsTGCGGGCGGCATCCCC
MANE Select
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NP_004272.2:p.Leu260=
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