ENST00000477226.6:n.859C>G
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ENST00000683013.1:n.773C>G
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ENST00000373960.4:c.1385C>G
MANE Select
|
ENSP00000363071.3:p.Ala462Gly
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ENST00000373960.3:c.1385C>G
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ENSP00000363071.3:p.Ala462Gly
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ENST00000483395.1:n.240C>G
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NM_001927.3:c.1385C>G , LRG_380t1:c.1385C>G
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NP_001918.3:p.Ala462Gly
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NM_001927.4:c.1385C>G
MANE Select
|
NP_001918.3:p.Ala462Gly
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NM_001382708.1:c.1382C>G
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NP_001369637.1:p.Ala461Gly
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NM_001382709.1:c.953C>G
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NP_001369638.1:p.Ala318Gly
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NM_001382710.1:c.1316C>G
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NP_001369639.1:p.Ala439Gly
|
|
NM_001382711.1:c.1364C>G
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NP_001369640.1:p.Ala455Gly
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NM_001382712.1:c.1371+217C>G
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NP_001369641.1:n.1371+217C>G
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NM_001382713.1:c.1115C>G
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NP_001369642.1:p.Ala372Gly
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