| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145457.2 | 406 | Missense Mutation | CGC,CTC | R91L | NP_001138929.2 |
| NM_001145458.2 | 406 | Missense Mutation | CGC,CTC | R91L | NP_001138930.2 |
| NM_001242356.2 | 406 | Intron | NP_001229285.1 | ||
| NM_001242357.2 | 406 | Intron | NP_001229286.1 | ||
| NM_004829.6 | 406 | Missense Mutation | CGC,CTC | R91L | NP_004820.2 |
| XM_011527528.2 | 406 | Missense Mutation | CGC,CTC | R91L | XP_011525830.1 |
| XM_011527529.2 | 406 | Missense Mutation | CGC,CTC | R91L | XP_011525831.1 |
| XM_011527530.2 | 406 | Missense Mutation | CGC,CTC | R91L | XP_011525832.1 |