ENST00000477226.6:n.566G>T
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ENST00000683013.1:n.480G>T
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ENST00000373960.4:c.1092G>T
MANE Select
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ENSP00000363071.3:p.Gln364His
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ENST00000373960.3:c.1092G>T
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ENSP00000363071.3:p.Gln364His
|
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ENST00000477226.5:n.564G>T
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|
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ENST00000492726.1:n.487G>T
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NM_001927.3:c.1092G>T , LRG_380t1:c.1092G>T
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NP_001918.3:p.Gln364His
|
|
NM_001927.4:c.1092G>T
MANE Select
|
NP_001918.3:p.Gln364His
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NM_001382708.1:c.1089G>T
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NP_001369637.1:p.Gln363His
|
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NM_001382709.1:c.736-76G>T
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NP_001369638.1:n.736-76G>T
|
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NM_001382710.1:c.1024-1G>T
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NP_001369639.1:n.1024-1G>T
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NM_001382711.1:c.1071G>T
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NP_001369640.1:p.Gln357His
|
|
NM_001382712.1:c.1092G>T
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NP_001369641.1:p.Gln364His
|
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NM_001382713.1:c.822G>T
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NP_001369642.1:p.Gln274His
|
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