ENST00000375128.5:c.715A>T
MANE Select
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ENSP00000364270.5:p.Thr239Ser
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ENST00000375128.4:c.715A>T
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ENSP00000364270.4:p.Thr239Ser
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ENST00000462523.5:c.*151A>T
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ENSP00000433006.1:n.*151A>T
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ENST00000485042.1:n.227A>T
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NM_000380.3:c.715A>T , LRG_471t1:c.715A>T
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NP_000371.1:p.Thr239Ser
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NR_027302.1:n.1063A>T
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XM_006717278.1:c.715A>T
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XP_006717341.1:p.Thr239Ser
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XM_011518988.1:c.715A>T
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XP_011517290.1:p.Thr239Ser
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XR_929839.1:n.1246A>T
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NM_001354975.1:c.589A>T
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NP_001341904.1:p.Thr197Ser
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NR_149091.1:n.560A>T
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NR_149092.1:n.726A>T
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NR_149093.1:n.1252A>T
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NR_149094.1:n.1146A>T
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NM_000380.4:c.715A>T
MANE Select
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NP_000371.1:p.Thr239Ser
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NM_001354975.2:c.589A>T
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NP_001341904.1:p.Thr197Ser
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NR_027302.2:n.994A>T
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NR_149091.2:n.491A>T
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NR_149092.2:n.657A>T
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NR_149093.2:n.1183A>T
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NR_149094.2:n.1077A>T
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