ENST00000477226.6:n.603C>G
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ENST00000683013.1:n.517C>G
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ENST00000373960.4:c.1129C>G
MANE Select
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ENSP00000363071.3:p.Leu377Val
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ENST00000373960.3:c.1129C>G
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ENSP00000363071.3:p.Leu377Val
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ENST00000477226.5:n.601C>G
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|
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ENST00000492726.1:n.524C>G
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NM_001927.3:c.1129C>G , LRG_380t1:c.1129C>G
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NP_001918.3:p.Leu377Val
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|
NM_001927.4:c.1129C>G
MANE Select
|
NP_001918.3:p.Leu377Val
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NM_001382708.1:c.1126C>G
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NP_001369637.1:p.Leu376Val
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NM_001382709.1:c.736-39C>G
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NP_001369638.1:n.736-39C>G
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NM_001382710.1:c.1060C>G
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NP_001369639.1:p.Leu354Val
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NM_001382711.1:c.1108C>G
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NP_001369640.1:p.Leu370Val
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NM_001382712.1:c.1129C>G
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NP_001369641.1:p.Leu377Val
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NM_001382713.1:c.859C>G
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NP_001369642.1:p.Leu287Val
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