ENST00000477226.6:n.612G>T
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ENST00000683013.1:n.526G>T
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ENST00000373960.4:c.1138G>T
MANE Select
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ENSP00000363071.3:p.Glu380Ter
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ENST00000373960.3:c.1138G>T
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ENSP00000363071.3:p.Glu380Ter
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ENST00000477226.5:n.610G>T
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ENST00000492726.1:n.533G>T
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NM_001927.3:c.1138G>T , LRG_380t1:c.1138G>T
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NP_001918.3:p.Glu380Ter
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NM_001927.4:c.1138G>T
MANE Select
|
NP_001918.3:p.Glu380Ter
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NM_001382708.1:c.1135G>T
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NP_001369637.1:p.Glu379Ter
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NM_001382709.1:c.736-30G>T
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NP_001369638.1:n.736-30G>T
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NM_001382710.1:c.1069G>T
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NP_001369639.1:p.Glu357Ter
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NM_001382711.1:c.1117G>T
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NP_001369640.1:p.Glu373Ter
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NM_001382712.1:c.1138G>T
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NP_001369641.1:p.Glu380Ter
|
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NM_001382713.1:c.868G>T
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NP_001369642.1:p.Glu290Ter
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