ENST00000253122.10:c.1142G>T
MANE Select
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ENSP00000253122.5:p.Gly381Val
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ENST00000253122.9:c.1142G>T
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ENSP00000253122.5:p.Gly381Val
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ENST00000413787.1:c.258-299G>T
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ENSP00000400463.1:n.258-299G>T
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ENST00000430077.6:c.797G>T
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ENSP00000403041.2:p.Gly266Val
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ENST00000442457.1:c.196G>T
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ENST00000457723.1:c.126G>T
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ENSP00000394742.1:p.Arg42Ser
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ENST00000467402.1:n.241G>T
|
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ENST00000485324.1:n.1175G>T
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NM_001142805.1:c.1112G>T
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NP_001136277.1:p.Gly371Val
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NM_001142806.1:c.797G>T
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NP_001136278.1:p.Gly266Val
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NM_005629.3:c.1142G>T
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NP_005620.1:p.Gly381Val
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NM_005629.4:c.1142G>T
MANE Select
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NP_005620.1:p.Gly381Val
|
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NM_001142805.2:c.1112G>T
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NP_001136277.1:p.Gly371Val
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