ENST00000367698.4:c.771del
MANE Select
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ENSP00000356671.3:p.Trp257Ter
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ENST00000367698.3:c.771del
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ENSP00000356671.3:p.Trp257Ter
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ENST00000487183.1:n.422del
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|
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ENST00000617423.4:c.559+1930del
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ENSP00000478688.1:n.559+1930del
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NM_000488.3:c.771del , LRG_577t1:c.771del
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NP_000479.1:p.Trp257Ter
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XM_005245198.2:c.627del
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XP_005245255.1:p.Trp209Ter
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NM_001365052.1:c.627del
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NP_001351981.1:p.Trp209Ter
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NM_000488.4:c.771del
MANE Select
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NP_000479.1:p.Trp257Ter
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NM_001365052.2:c.627del
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NP_001351981.1:p.Trp209Ter
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NM_001386302.1:c.894del
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NP_001373231.1:p.Trp298Ter
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NM_001386303.1:c.852del
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NP_001373232.1:p.Trp284Ter
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NM_001386304.1:c.750del
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NP_001373233.1:p.Trp250Ter
|
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NM_001386305.1:c.763-49del
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NP_001373234.1:n.763-49del
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NM_001386306.1:c.555del
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NP_001373235.1:p.Trp185Ter
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