A G-to-A point mutation at coding nucleotide 1159/1954/1984 of the cDNA (NM_080465/ENSMUST00000066890/NM_001312905) results in a valine to isoleucine substitution at position 387/652/662 of the encoded protein (NP_536713:p.V387I, ENSMUSP00000067884:p.V652I, NP_001299834:p.V662I). (J:222308)