ENST00000375128.5:c.778A>T
MANE Select
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ENSP00000364270.5:p.Thr260Ser
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ENST00000375128.4:c.778A>T
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ENSP00000364270.4:p.Thr260Ser
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ENST00000462523.5:c.*214A>T
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ENSP00000433006.1:n.*214A>T
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ENST00000485042.1:n.290A>T
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NM_000380.3:c.778A>T , LRG_471t1:c.778A>T
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NP_000371.1:p.Thr260Ser
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NR_027302.1:n.1126A>T
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XM_006717278.1:c.772+6A>T
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XP_006717341.1:n.772+6A>T
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XM_011518988.1:c.772+6A>T
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XP_011517290.1:n.772+6A>T
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NM_001354975.1:c.652A>T
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NP_001341904.1:p.Thr218Ser
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NR_149091.1:n.623A>T
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NR_149092.1:n.789A>T
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NR_149093.1:n.1315A>T
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|
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NR_149094.1:n.1209A>T
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|
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NM_000380.4:c.778A>T
MANE Select
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NP_000371.1:p.Thr260Ser
|
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NM_001354975.2:c.652A>T
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NP_001341904.1:p.Thr218Ser
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NR_027302.2:n.1057A>T
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|
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NR_149091.2:n.554A>T
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NR_149092.2:n.720A>T
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|
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NR_149093.2:n.1246A>T
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NR_149094.2:n.1140A>T
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