| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003057.2 | 416 | Missense Mutation | CAC,CGC | H90R | NP_003048.1 |
| NM_153187.1 | 416 | Missense Mutation | CAC,CGC | H90R | NP_694857.1 |
| XM_005267102.4 | 416 | Missense Mutation | CAC,CGC | H90R | XP_005267159.1 |
| XM_005267103.1 | 416 | Missense Mutation | CAC,CGC | H90R | XP_005267160.1 |
| XM_005267104.4 | 416 | Intron | XP_005267161.1 | ||
| XM_005267105.4 | 416 | Intron | XP_005267162.1 | ||
| XM_006715552.1 | 416 | Missense Mutation | CAC,CGC | H90R | XP_006715615.1 |
| XM_011536074.2 | 416 | Intron | XP_011534376.1 |