ENST00000477226.6:n.858G>T
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ENST00000683013.1:n.772G>T
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ENST00000373960.4:c.1384G>T
MANE Select
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ENSP00000363071.3:p.Ala462Ser
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ENST00000373960.3:c.1384G>T
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ENSP00000363071.3:p.Ala462Ser
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ENST00000483395.1:n.239G>T
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NM_001927.3:c.1384G>T , LRG_380t1:c.1384G>T
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NP_001918.3:p.Ala462Ser
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NM_001927.4:c.1384G>T
MANE Select
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NP_001918.3:p.Ala462Ser
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NM_001382708.1:c.1381G>T
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NP_001369637.1:p.Ala461Ser
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NM_001382709.1:c.952G>T
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NP_001369638.1:p.Ala318Ser
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NM_001382710.1:c.1315G>T
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NP_001369639.1:p.Ala439Ser
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NM_001382711.1:c.1363G>T
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NP_001369640.1:p.Ala455Ser
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NM_001382712.1:c.1371+216G>T
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NP_001369641.1:n.1371+216G>T
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NM_001382713.1:c.1114G>T
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NP_001369642.1:p.Ala372Ser
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