ENST00000309755.9:c.1022G>T
MANE Select
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ENSP00000312397.4:p.Gly341Val
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ENST00000309755.8:c.1022G>T
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ENSP00000312397.4:p.Gly341Val
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ENST00000502381.1:n.609G>T
|
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ENST00000504208.5:c.*335-10713G>T
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ENSP00000423585.1:n.*335-10713G>T
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ENST00000505853.1:c.902G>T
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ENSP00000426173.1:p.Gly301Val
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ENST00000506491.5:c.776G>T
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ENSP00000424828.1:p.Gly259Val
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ENST00000506873.5:n.647G>T
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ENST00000508657.5:c.926G>T
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ENSP00000422099.1:p.Gly309Val
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NM_001257194.1:c.926G>T
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NP_001244123.1:p.Gly309Val
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NM_001257195.1:c.776G>T
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NP_001244124.1:p.Gly259Val
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NM_017415.2:c.1022G>T
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NP_059111.2:p.Gly341Val
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NM_017415.3:c.1022G>T
MANE Select
|
NP_059111.2:p.Gly341Val
|
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NM_001257195.2:c.776G>T
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NP_001244124.1:p.Gly259Val
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