ENST00000374580.10:c.2640_2643delinsTGAA
MANE Select
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ENSP00000363708.4:p.Asp880=
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ENST00000638587.1:c.2571_2574delinsTGAA
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ENSP00000491062.1:n.2571_2574delinsTGAA
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ENST00000374574.2:c.1587-3391_1587-3388delinsTGAA
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ENSP00000363702.2:n.1587-3391_1587-3388delinsTGAA
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ENST00000374580.8:c.2640_2643delinsTGAA
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ENSP00000363708.4:p.Asp880=
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NM_001204.6:c.2640_2643delinsTGAA , LRG_712t1:c.2640_2643delinsTGAA
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NP_001195.2:p.Asp880=
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XM_011511687.1:c.2640_2643delinsTGAA
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XP_011509989.1:p.Asp880=
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XM_011511688.1:c.1587-3391_1587-3388delinsTGAA
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XP_011509990.1:n.1587-3391_1587-3388delinsTGAA
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NM_001204.7:c.2640_2643delinsTGAA
MANE Select
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NP_001195.2:p.Asp880=
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