ENST00000698727.1:n.1656G>T
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ENST00000698728.1:n.2175G>T
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ENST00000698729.1:n.3721G>T
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ENST00000698730.1:n.3721G>T
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|
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ENST00000698731.1:c.2455G>T
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ENSP00000513898.1:p.Ala819Ser
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ENST00000698732.1:c.*1457G>T
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ENSP00000513899.1:n.*1457G>T
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ENST00000698733.1:c.*1783G>T
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ENSP00000513900.1:n.*1783G>T
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ENST00000698734.1:c.2596G>T
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ENSP00000513901.1:p.Ala866Ser
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ENST00000698735.1:n.2711G>T
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ENST00000698736.1:n.2711G>T
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ENST00000698737.1:n.2711G>T
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ENST00000698738.1:n.2711G>T
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ENST00000698739.1:n.2711G>T
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ENST00000372371.8:c.2596G>T
MANE Select
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ENSP00000361446.3:p.Ala866Ser
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ENST00000372371.7:c.2596G>T
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ENSP00000361446.3:p.Ala866Ser
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ENST00000472014.5:n.469+4715G>T
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NM_007055.3:c.2596G>T
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NP_008986.2:p.Ala866Ser
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NM_007055.4:c.2596G>T
MANE Select
|
NP_008986.2:p.Ala866Ser
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