ENST00000477226.6:n.709A>T
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ENST00000683013.1:n.623A>T
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ENST00000373960.4:c.1235A>T
MANE Select
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ENSP00000363071.3:p.Glu412Val
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ENST00000373960.3:c.1235A>T
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ENSP00000363071.3:p.Glu412Val
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ENST00000477226.5:n.707A>T
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ENST00000492726.1:n.630A>T
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NM_001927.3:c.1235A>T , LRG_380t1:c.1235A>T
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NP_001918.3:p.Glu412Val
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NM_001927.4:c.1235A>T
MANE Select
|
NP_001918.3:p.Glu412Val
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NM_001382708.1:c.1232A>T
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NP_001369637.1:p.Glu411Val
|
|
NM_001382709.1:c.803A>T
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NP_001369638.1:p.Glu268Val
|
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NM_001382710.1:c.1166A>T
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NP_001369639.1:p.Glu389Val
|
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NM_001382711.1:c.1214A>T
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NP_001369640.1:p.Glu405Val
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NM_001382712.1:c.1235A>T
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NP_001369641.1:p.Glu412Val
|
|
NM_001382713.1:c.965A>T
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NP_001369642.1:p.Glu322Val
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