| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001079528.3 | 4395 | Intron | NP_001072996.1 | ||
| NM_001171.5 | 4395 | Missense Mutation | CAC,CGC | H1461R | NP_001162.4 |
| XM_011522479.2 | 4395 | Missense Mutation | CAC,CGC | H1450R | XP_011520781.1 |
| XM_011522480.1 | 4395 | Missense Mutation | CAC,CGC | H1347R | XP_011520782.1 |
| XM_011522481.2 | 4395 | Missense Mutation | CAC,CGC | H1347R | XP_011520783.1 |
| XM_011522482.2 | 4395 | Intron | XP_011520784.1 | ||
| XM_017023212.1 | 4395 | Missense Mutation | CAC,CGC | H1405R | XP_016878701.1 |
| XM_017023213.1 | 4395 | Missense Mutation | CAC,CGC | H1347R | XP_016878702.1 |
| XM_017023214.1 | 4395 | Intron | XP_016878703.1 |