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Mutations on the Protein: P54098 From Positions: 1177 To 1239

4
3
1
0


Swiss-Prot Disease: VAR_058897
p.ASP1184ASN
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB)


Swiss-Prot Disease: VAR_065119
p.ASP1186HIS
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1 (PEOA1)


dbSNP Polymorphism: rs3087374
p.GLN1236HIS
N/A
N/A


Swiss-Prot Disease: VAR_058898
p.LYS1191ASN
N/A
N/A
Mitochondrial DNA depletion syndrome 4A (MTDPS4A)






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