ENST00000367698.4:c.1021_1025delinsGATGA
MANE Select
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ENSP00000356671.3:p.Asp341=
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ENST00000367698.3:c.1021_1025delinsGATGA
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ENSP00000356671.3:p.Asp341=
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ENST00000617423.4:c.559+2180_559+2184delinsGATGA
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ENSP00000478688.1:n.559+2180_559+2184delinsGATGA
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NM_000488.3:c.1021_1025delinsGATGA , LRG_577t1:c.1021_1025delinsGATGA
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NP_000479.1:p.Asp341=
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XM_005245198.2:c.877_881delinsGATGA
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XP_005245255.1:p.Asp293=
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NM_001365052.1:c.877_881delinsGATGA
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NP_001351981.1:p.Asp293=
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NM_000488.4:c.1021_1025delinsGATGA
MANE Select
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NP_000479.1:p.Asp341=
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NM_001365052.2:c.877_881delinsGATGA
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NP_001351981.1:p.Asp293=
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NM_001386302.1:c.1144_1148delinsGATGA
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NP_001373231.1:p.Asp382=
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NM_001386303.1:c.1102_1106delinsGATGA
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NP_001373232.1:p.Asp368=
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NM_001386304.1:c.1000_1004delinsGATGA
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NP_001373233.1:p.Asp334=
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NM_001386305.1:c.964_968delinsGATGA
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NP_001373234.1:p.Asp322=
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NM_001386306.1:c.805_809delinsGATGA
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NP_001373235.1:p.Asp269=
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