ENST00000477226.6:n.678A>G
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ENST00000683013.1:n.592A>G
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ENST00000373960.4:c.1204A>G
MANE Select
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ENSP00000363071.3:p.Ile402Val
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ENST00000373960.3:c.1204A>G
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ENSP00000363071.3:p.Ile402Val
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ENST00000477226.5:n.676A>G
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ENST00000492726.1:n.599A>G
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NM_001927.3:c.1204A>G , LRG_380t1:c.1204A>G
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NP_001918.3:p.Ile402Val
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NM_001927.4:c.1204A>G
MANE Select
|
NP_001918.3:p.Ile402Val
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NM_001382708.1:c.1201A>G
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NP_001369637.1:p.Ile401Val
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NM_001382709.1:c.772A>G
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NP_001369638.1:p.Ile258Val
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NM_001382710.1:c.1135A>G
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NP_001369639.1:p.Ile379Val
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NM_001382711.1:c.1183A>G
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NP_001369640.1:p.Ile395Val
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NM_001382712.1:c.1204A>G
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NP_001369641.1:p.Ile402Val
|
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NM_001382713.1:c.934A>G
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NP_001369642.1:p.Ile312Val
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