| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_019005.3 | 498 | Missense Mutation | AAT,CAT | N122H | NP_061878.3 |
| XM_005249780.3 | 498 | Missense Mutation | AAT,CAT | N122H | XP_005249837.1 |
| XM_005249781.3 | 498 | Missense Mutation | AAT,CAT | N122H | XP_005249838.1 |
| XM_005249782.3 | 498 | Missense Mutation | AAT,CAT | N122H | XP_005249839.1 |
| XM_005249784.3 | 498 | Missense Mutation | AAT,CAT | N122H | XP_005249841.1 |
| XM_011515432.2 | 498 | Missense Mutation | AAT,CAT | N122H | XP_011513734.1 |
| XM_017012361.1 | 498 | Missense Mutation | AAT,CAT | N122H | XP_016867850.1 |
| XM_017012362.1 | 498 | UTR 5 | XP_016867851.1 |