ENST00000477226.6:n.779A>T
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|
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ENST00000683013.1:n.693A>T
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|
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ENST00000373960.4:c.1305A>T
MANE Select
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ENSP00000363071.3:p.Gln435His
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ENST00000373960.3:c.1305A>T
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ENSP00000363071.3:p.Gln435His
|
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ENST00000483395.1:n.160A>T
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NM_001927.3:c.1305A>T , LRG_380t1:c.1305A>T
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NP_001918.3:p.Gln435His
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NM_001927.4:c.1305A>T
MANE Select
|
NP_001918.3:p.Gln435His
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NM_001382708.1:c.1302A>T
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NP_001369637.1:p.Gln434His
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NM_001382709.1:c.873A>T
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NP_001369638.1:p.Gln291His
|
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NM_001382710.1:c.1236A>T
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NP_001369639.1:p.Gln412His
|
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NM_001382711.1:c.1284A>T
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NP_001369640.1:p.Gln428His
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NM_001382712.1:c.1305A>T
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NP_001369641.1:p.Gln435His
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|
NM_001382713.1:c.1035A>T
|
NP_001369642.1:p.Gln345His
|
|