ENST00000265631.10:c.1903_1919delinsGATCACGTTGGGGGCTA
MANE Select
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ENSP00000265631.6:p.Asp635=
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ENST00000265631.9:c.1903_1919delinsGATCACGTTGGGGGCTA
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ENSP00000265631.5:p.Asp635=
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ENST00000416240.6:c.1906_1922delinsGATCACGTTGGGGGCTA
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ENSP00000400101.2:p.Asp636=
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ENST00000494085.1:n.406_422delinsGATCACGTTGGGGGCTA
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NM_001160210.1:c.1906_1922delinsGATCACGTTGGGGGCTA
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NP_001153682.1:p.Asp636=
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NM_014251.2:c.1903_1919delinsGATCACGTTGGGGGCTA
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NP_055066.1:p.Asp635=
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NR_027662.1:n.1978_1994delinsGATCACGTTGGGGGCTA
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XM_006715831.2:c.1936_1952delinsGATCACGTTGGGGGCTA
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XP_006715894.1:p.Asp646=
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XM_011515728.1:c.1051_1067delinsGATCACGTTGGGGGCTA
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XP_011514030.1:p.Asp351=
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XM_006715831.4:c.1936_1952delinsGATCACGTTGGGGGCTA
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XP_006715894.1:p.Asp646=
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XM_017011663.1:c.1894_1910delinsGATCACGTTGGGGGCTA
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XP_016867152.1:p.Asp632=
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XM_017011664.2:c.1051_1067delinsGATCACGTTGGGGGCTA
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XP_016867153.1:p.Asp351=
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XM_017011665.1:c.1051_1067delinsGATCACGTTGGGGGCTA
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XP_016867154.1:p.Asp351=
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XR_001744525.2:n.2149_2165delinsGATCACGTTGGGGGCTA
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XR_002956405.1:n.2707_2723delinsGATCACGTTGGGGGCTA
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NM_014251.3:c.1903_1919delinsGATCACGTTGGGGGCTA
MANE Select
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NP_055066.1:p.Asp635=
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NR_027662.2:n.1929_1945delinsGATCACGTTGGGGGCTA
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NM_001160210.2:c.1906_1922delinsGATCACGTTGGGGGCTA
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NP_001153682.1:p.Asp636=
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