CGT16786539TGG
CGT>TGG
R1844W | Mhc-PA; R1844W | Mhc-PB; R1844W | Mhc-PC; R1844W | Mhc-PD; R1844W | Mhc-PE; R1844W | Mhc-PF; R1844W | Mhc-PG; R1844W | Mhc-PH; R1844W | Mhc-PI; R1844W | Mhc-PK; R1844W | Mhc-PL; R1844W | Mhc-PM; R1844W | Mhc-PN; R1844W | Mhc-PO; R1844W | Mhc-PP; R1844W | Mhc-PQ; R1844W | Mhc-PR; R1844W | Mhc-PS; R1844W | Mhc-PT; R1844W | Mhc-PU; R1844W | Mhc-PV
R1844W
Analogous R1845W mutation in human MYH7 implicated in myopathy; mutation carried on in vitro construct.