ENST00000233575.7:c.692A>T
MANE Select
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ENSP00000233575.2:p.Asp231Val
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ENST00000233575.6:c.692A>T
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ENSP00000233575.2:p.Asp231Val
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ENST00000427123.5:c.*502A>T
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ENSP00000405399.1:n.*502A>T
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ENST00000440760.5:c.*537A>T
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ENSP00000399727.1:n.*537A>T
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ENST00000453453.1:c.*219A>T
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ENSP00000401922.1:n.*219A>T
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ENST00000493711.1:n.409A>T
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|
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ENST00000494893.5:n.868A>T
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ENST00000537606.5:c.617A>T
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ENSP00000439208.1:p.Asp206Val
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NM_001267059.1:c.656A>T
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NP_001253988.1:p.Asp219Val
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NM_001267060.1:c.617A>T
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NP_001253989.1:p.Asp206Val
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NM_001267061.1:c.632A>T
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NP_001253990.1:p.Asp211Val
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NM_014748.3:c.692A>T
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NP_055563.1:p.Asp231Val
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NR_049782.1:n.1065A>T
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|
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NR_049783.1:n.1038A>T
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|
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NR_049784.1:n.1014A>T
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|
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NR_049785.1:n.947A>T
|
|
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NR_049786.1:n.896A>T
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|
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NR_049787.1:n.747A>T
|
|
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NR_049788.1:n.677A>T
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|
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XM_011533203.1:c.50A>T
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XP_011531505.1:p.Asp17Val
|
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XM_011533203.2:c.50A>T
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XP_011531505.1:p.Asp17Val
|
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XM_017005405.2:c.50A>T
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XP_016860894.1:p.Asp17Val
|
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NM_014748.4:c.692A>T
MANE Select
|
NP_055563.1:p.Asp231Val
|
|
NM_001267059.2:c.656A>T
|
NP_001253988.1:p.Asp219Val
|
|
NM_001267061.2:c.632A>T
|
NP_001253990.1:p.Asp211Val
|
|
NR_049782.2:n.945A>T
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|
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NR_049783.2:n.918A>T
|
|
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NR_049784.2:n.894A>T
|
|
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NR_049785.2:n.827A>T
|
|
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NR_049786.2:n.776A>T
|
|
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NR_049787.2:n.627A>T
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|
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NR_049788.2:n.557A>T
|
|
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NM_001267060.2:c.617A>T
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NP_001253989.1:p.Asp206Val
|
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