ENST00000400521.7:c.1163A>T
MANE Select
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ENSP00000383365.1:p.Asp388Val
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ENST00000400518.5:c.1073A>T
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ENSP00000383362.1:p.Asp358Val
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ENST00000400519.6:c.1160A>T
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ENSP00000383363.1:p.Asp387Val
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ENST00000400521.6:c.1163A>T
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ENSP00000383365.1:p.Asp388Val
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ENST00000400525.6:c.1094A>T
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ENSP00000383369.3:p.Asp365Val
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ENST00000462330.5:c.86A>T
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ENSP00000485603.2:p.Asp29Val
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ENST00000462843.2:c.113A>T
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ENSP00000485466.2:p.Asp38Val
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ENST00000474308.5:c.1106A>T
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ENSP00000485665.1:p.Asp369Val
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ENST00000485358.5:c.131A>T
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ENSP00000485499.2:p.Asp44Val
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ENST00000487165.5:n.1257A>T
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ENST00000494454.5:n.1237A>T
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|
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ENST00000495655.2:n.707A>T
|
|
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ENST00000542719.6:c.875A>T
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ENSP00000485128.2:p.Asp292Val
|
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ENST00000634471.1:n.244-370A>T
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|
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ENST00000634537.1:c.392A>T
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ENSP00000489208.1:p.Asp131Val
|
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NM_006440.4:c.1163A>T
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NP_006431.2:p.Asp388Val
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NM_001352300.1:c.1160A>T
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NP_001339229.1:p.Asp387Val
|
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NM_001352301.1:c.1073A>T
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NP_001339230.1:p.Asp358Val
|
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NM_001352302.1:c.875A>T
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NP_001339231.1:p.Asp292Val
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NR_147957.1:n.1295A>T
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|
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NM_006440.5:c.1163A>T
MANE Select
|
NP_006431.2:p.Asp388Val
|
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NM_001352300.2:c.1160A>T
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NP_001339229.1:p.Asp387Val
|
|
NR_147957.2:n.1121A>T
|
|
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NM_001352301.2:c.1073A>T
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NP_001339230.1:p.Asp358Val
|
|
NM_001352302.2:c.875A>T
|
NP_001339231.1:p.Asp292Val
|
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