ENST00000477226.6:n.869G>T
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ENST00000683013.1:n.783G>T
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ENST00000373960.4:c.1395G>T
MANE Select
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ENSP00000363071.3:p.Gln465His
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ENST00000373960.3:c.1395G>T
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ENSP00000363071.3:p.Gln465His
|
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ENST00000483395.1:n.250G>T
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NM_001927.3:c.1395G>T , LRG_380t1:c.1395G>T
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NP_001918.3:p.Gln465His
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NM_001927.4:c.1395G>T
MANE Select
|
NP_001918.3:p.Gln465His
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NM_001382708.1:c.1392G>T
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NP_001369637.1:p.Gln464His
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NM_001382709.1:c.963G>T
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NP_001369638.1:p.Gln321His
|
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NM_001382710.1:c.1326G>T
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NP_001369639.1:p.Gln442His
|
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NM_001382711.1:c.1374G>T
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NP_001369640.1:p.Gln458His
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NM_001382712.1:c.1371+227G>T
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NP_001369641.1:n.1371+227G>T
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NM_001382713.1:c.1125G>T
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NP_001369642.1:p.Gln375His
|
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