Figure 3
From: Carrier re-sequencing reveals rare but benign variants in recessive deafness genes

Multi-species sequence alignments of amino acids A434 in SLC26A4, R266 in LOXHD1, V1299 in CDH23, K96 in MYO15A and T123 in GJB2.
From: Carrier re-sequencing reveals rare but benign variants in recessive deafness genes
Multi-species sequence alignments of amino acids A434 in SLC26A4, R266 in LOXHD1, V1299 in CDH23, K96 in MYO15A and T123 in GJB2.