| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020824.3 | 4770 | Intron | NP_065875.3 | ||
| XM_005252542.3 | 4770 | Intron | XP_005252599.1 | ||
| XM_005252544.4 | 4770 | Missense Mutation | CAA,GAA | Q1331E | XP_005252601.1 |
| XM_011519602.2 | 4770 | Missense Mutation | CAA,GAA | Q1375E | XP_011517904.1 |
| XM_011519603.2 | 4770 | Missense Mutation | CAA,GAA | Q1375E | XP_011517905.1 |
| XM_011519604.2 | 4770 | Intron | XP_011517906.1 | ||
| XM_011519605.2 | 4770 | Missense Mutation | CAA,GAA | Q1365E | XP_011517907.1 |
| XM_011519606.2 | 4770 | Missense Mutation | CAA,GAA | Q1307E | XP_011517908.1 |
| XM_011519607.2 | 4770 | Missense Mutation | CAA,GAA | Q1375E | XP_011517909.1 |
| XM_017016459.1 | 4770 | Missense Mutation | CAA,GAA | Q1341E | XP_016871948.1 |
| XM_017016460.1 | 4770 | Missense Mutation | CAA,GAA | Q1331E | XP_016871949.1 |
| XM_017016461.1 | 4770 | Intron | XP_016871950.1 |