ENST00000253122.10:c.1163C>T
MANE Select
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ENSP00000253122.5:p.Ala388Val
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ENST00000253122.9:c.1163C>T
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ENSP00000253122.5:p.Ala388Val
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ENST00000413787.1:c.258-278C>T
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ENSP00000400463.1:n.258-278C>T
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ENST00000430077.6:c.818C>T
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ENSP00000403041.2:p.Ala273Val
|
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ENST00000442457.1:c.217C>T
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|
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ENST00000457723.1:c.147C>T
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ENSP00000394742.1:p.Arg49=
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ENST00000467402.1:n.262C>T
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|
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ENST00000485324.1:n.1196C>T
|
|
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NM_001142805.1:c.1133C>T
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NP_001136277.1:p.Ala378Val
|
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NM_001142806.1:c.818C>T
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NP_001136278.1:p.Ala273Val
|
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NM_005629.3:c.1163C>T
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NP_005620.1:p.Ala388Val
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NM_005629.4:c.1163C>T
MANE Select
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NP_005620.1:p.Ala388Val
|
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NM_001142805.2:c.1133C>T
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NP_001136277.1:p.Ala378Val
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