| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001198810.1 | 1321 | Missense Mutation | CAC,CGC | H409R | NP_001185739.1 |
| NM_003627.5 | 1321 | Missense Mutation | CAC,CGC | H409R | NP_003618.1 |
| XM_005274358.4 | 1321 | Missense Mutation | CAC,CGC | H425R | XP_005274415.1 |
| XM_011545320.2 | 1321 | Missense Mutation | CAC,CGC | H394R | XP_011543622.1 |
| XM_011545321.2 | 1321 | Missense Mutation | CAC,CGC | H153R | XP_011543623.1 |
| XM_011545322.1 | 1321 | Missense Mutation | CAC,CGC | H153R | XP_011543624.1 |
| XM_017018451.1 | 1321 | Missense Mutation | CAC,CGC | H409R | XP_016873940.1 |
| XM_017018452.1 | 1321 | Missense Mutation | CAC,CGC | H378R | XP_016873941.1 |
| XM_017018453.1 | 1321 | Missense Mutation | CAC,CGC | H153R | XP_016873942.1 |