| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040283.2 | 242 | Missense Mutation | CAC,CGC | H46R | NP_001035373.1 |
| XM_011527214.1 | 242 | UTR 5 | XP_011525516.1 | ||
| XM_011527215.1 | 242 | UTR 5 | XP_011525517.1 | ||
| XM_011527216.2 | 242 | Missense Mutation | CAC,CGC | H51R | XP_011525518.1 |
| XM_017027123.1 | 242 | Missense Mutation | CAC,CGC | H51R | XP_016882612.1 |
| XM_017027124.1 | 242 | Missense Mutation | CAC,CGC | H49R | XP_016882613.1 |
| XM_017027125.1 | 242 | Missense Mutation | CAC,CGC | H46R | XP_016882614.1 |
| XM_017027126.1 | 242 | Missense Mutation | CAC,CGC | H46R | XP_016882615.1 |
| XM_017027127.1 | 242 | Missense Mutation | CAC,CGC | H46R | XP_016882616.1 |
| XM_017027128.1 | 242 | Missense Mutation | CAC,CGC | H46R | XP_016882617.1 |
| XM_017027129.1 | 242 | Missense Mutation | CAC,CGC | H51R | XP_016882618.1 |