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Mutations on the Protein: P68133 From Positions: 151 To 170

5
3
0
2






Swiss-Prot Disease: VAR_062447
p.ASP156ASN
N/A
N/A
Nemaline myopathy 3 (NEM3)


Swiss-Prot Disease: VAR_011684
p.VAL165LEU
N/A
N/A
Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM)


Swiss-Prot Disease: VAR_062448
p.VAL165MET
N/A
N/A
Nemaline myopathy 3 (NEM3)


OMIM Disease: 102610.0004
p.VAL163LEU
N/A
N/A
NEMALINE MYOPATHY 3


OMIM Disease: 102610.0014
p.VAL163MET
N/A
N/A
NEMALINE MYOPATHY 3






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