| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020747.2 | 3788 | Missense Mutation | ACG,CCG | T1473P | NP_065798.2 |
| XM_005272037.2 | 3788 | Missense Mutation | ACG,CCG | T1473P | XP_005272094.1 |
| XM_005272038.1 | 3788 | Missense Mutation | ACG,CCG | T1473P | XP_005272095.1 |
| XM_005272039.2 | 3788 | Missense Mutation | ACG,CCG | T1473P | XP_005272096.1 |
| XM_005272040.3 | 3788 | Missense Mutation | ACG,CCG | T1185P | XP_005272097.1 |
| XM_011543520.2 | 3788 | Intron | XP_011541822.1 | ||
| XM_011543522.2 | 3788 | Missense Mutation | ACG,CCG | T1176P | XP_011541824.1 |
| XM_011543523.2 | 3788 | Missense Mutation | ACG,CCG | T1088P | XP_011541825.1 |
| XM_017009674.1 | 3788 | Missense Mutation | ACG,CCG | T1473P | XP_016865163.1 |