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Mutations on the Protein: P12235 From Positions: 89 To 104

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Swiss-Prot Disease: VAR_038814
p.ALA90ASP
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)


Swiss-Prot Disease: VAR_022460
p.ASP104GLY
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)


Swiss-Prot Disease: VAR_022459
p.LEU98PRO
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)


OMIM Disease: 103220.0004
p.ASP104GLY
N/A
N/A
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,||AUTOSOMAL DOMINANT, 2


OMIM Disease: 103220.0003
p.LEU98PRO
N/A
N/A
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,||AUTOSOMAL DOMINANT, 2






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