| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015470.2 | 3990 | Missense Mutation | AAC,CAC | N599H | NP_056285.1 |
| XM_005264251.3 | 3990 | Missense Mutation | AAC,CAC | N1164H | XP_005264308.1 |
| XM_005264252.3 | 3990 | Missense Mutation | AAC,CAC | N1270H | XP_005264309.1 |
| XM_005264253.4 | 3990 | Intron | XP_005264310.1 | ||
| XM_006711985.3 | 3990 | Missense Mutation | AAC,CAC | N1195H | XP_006712048.1 |
| XM_011532753.2 | 3990 | Missense Mutation | AAC,CAC | N1064H | XP_011531055.1 |
| XM_011532754.2 | 3990 | Intron | XP_011531056.1 | ||
| XM_011532755.2 | 3990 | Intron | XP_011531057.1 | ||
| XM_011532756.2 | 3990 | Intron | XP_011531058.1 | ||
| XM_017003788.1 | 3990 | Missense Mutation | AAC,CAC | N1019H | XP_016859277.1 |