| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206994.1 | 1274 | Missense Mutation | CAC,CGC | H392R | NP_001193923.1 |
| NM_001206995.1 | 1274 | Missense Mutation | CAC,CGC | H392R | NP_001193924.1 |
| NM_001206996.1 | 1274 | Missense Mutation | CAC,CGC | H382R | NP_001193925.1 |
| NM_020416.3 | 1274 | Missense Mutation | CAC,CGC | H399R | NP_065149.2 |
| NM_181876.2 | 1274 | Missense Mutation | CAC,CGC | H399R | NP_870991.1 |
| XM_005247979.4 | 1274 | Missense Mutation | CAC,CGC | H182R | XP_005248036.1 |
| XM_011513495.1 | 1274 | Missense Mutation | CAC,CGC | H385R | XP_011511797.1 |
| XM_011513496.1 | 1274 | Missense Mutation | CAC,CGC | H244R | XP_011511798.1 |