ENST00000324856.13:c.126G=
MANE Select
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ENSP00000320485.7:p.Ala42=
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ENST00000430799.7:c.-13+2912G=
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ENSP00000390317.3:n.-13+2912G=
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ENST00000637465.1:c.-13+429G=
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ENSP00000490650.1:n.-13+429G=
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ENST00000324856.11:c.126G=
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ENSP00000320485.7:p.Ala42=
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ENST00000457599.6:c.126G=
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ENSP00000387636.2:p.Ala42=
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NM_006015.4:c.126G= , LRG_875t1:c.126G=
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NP_006006.3:p.Ala42=
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NM_139135.2:c.126G=
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NP_624361.1:p.Ala42=
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NM_006015.5:c.126G=
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NP_006006.3:p.Ala42=
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NM_139135.3:c.126G=
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NP_624361.1:p.Ala42=
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NM_006015.6:c.126G=
MANE Select
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NP_006006.3:p.Ala42=
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NM_139135.4:c.126G=
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NP_624361.1:p.Ala42=
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