| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122838.1 | 1467 | Missense Mutation | CAT,CGT | H380R | NP_001116310.1 |
| NM_198990.4 | 1467 | Missense Mutation | CAT,CGT | H380R | NP_945341.3 |
| XM_005250214.4 | 1467 | Missense Mutation | CAT,CGT | H380R | XP_005250271.2 |
| XM_005250215.2 | 1467 | Missense Mutation | CAT,CGT | H380R | XP_005250272.1 |
| XM_005250218.2 | 1467 | Missense Mutation | CAT,CGT | H380R | XP_005250275.1 |
| XM_011515933.2 | 1467 | Missense Mutation | CAT,CGT | H380R | XP_011514235.1 |
| XM_011515934.2 | 1467 | Missense Mutation | CAT,CGT | H245R | XP_011514236.1 |
| XM_017011854.1 | 1467 | Missense Mutation | CAT,CGT | H380R | XP_016867343.1 |
| XM_017011855.1 | 1467 | Missense Mutation | CAT,CGT | H380R | XP_016867344.1 |
| XM_017011856.1 | 1467 | Intron | XP_016867345.1 | ||
| XM_017011857.1 | 1467 | Intron | XP_016867346.1 |