ENST00000269980.7:c.1175A>C
MANE Select
|
ENSP00000269980.2:p.Glu392Ala
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ENST00000269980.6:c.1175A>C
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ENSP00000269980.2:p.Glu392Ala
|
|
ENST00000457836.6:c.1184A>C
|
ENSP00000416000.2:p.Glu395Ala
|
|
ENST00000540732.3:c.1277A>C
|
ENSP00000443246.1:p.Glu426Ala
|
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ENST00000544905.1:c.62-57A>C
|
|
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ENST00000595085.5:c.922+1748A>C
|
ENSP00000471150.2:n.922+1748A>C
|
|
NM_000709.3:c.1175A>C
|
NP_000700.1:p.Glu392Ala
|
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NM_001164783.1:c.1172A>C
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NP_001158255.1:p.Glu391Ala
|
|
NM_000709.4:c.1175A>C
MANE Select
|
NP_000700.1:p.Glu392Ala
|
|
NM_001164783.2:c.1172A>C
|
NP_001158255.1:p.Glu391Ala
|
|