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Mutations on the Protein: NP_733822 From Positions: 476 To 507

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OMIM Disease: 150330.0010
p.ARG482GLN
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0012
p.ARG482LEU
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0011
p.ARG482TRP
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0038
p.GLN493TER
N/A
N/A
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B






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