| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145114.1 | 4011 | Missense Mutation | CAC,CGC | H1230R | NP_001138586.1 |
| NM_001284337.1 | 4011 | Missense Mutation | CAC,CGC | H1191R | NP_001271266.1 |
| NM_015179.3 | 4011 | Missense Mutation | CAC,CGC | H1291R | NP_055994.2 |
| XM_011539555.1 | 4011 | Missense Mutation | CAC,CGC | H1263R | XP_011537857.1 |
| XM_011539556.2 | 4011 | Intron | XP_011537858.1 |