| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001079528.3 | 4454 | Intron | NP_001072996.1 | ||
| NM_001171.5 | 4454 | Missense Mutation | AGC,GGC | S1481G | NP_001162.4 |
| XM_011522479.2 | 4454 | Missense Mutation | AGC,GGC | S1470G | XP_011520781.1 |
| XM_011522480.1 | 4454 | Missense Mutation | AGC,GGC | S1367G | XP_011520782.1 |
| XM_011522481.2 | 4454 | Missense Mutation | AGC,GGC | S1367G | XP_011520783.1 |
| XM_011522482.2 | 4454 | Intron | XP_011520784.1 | ||
| XM_017023212.1 | 4454 | Missense Mutation | AGC,GGC | S1425G | XP_016878701.1 |
| XM_017023213.1 | 4454 | Missense Mutation | AGC,GGC | S1367G | XP_016878702.1 |
| XM_017023214.1 | 4454 | Intron | XP_016878703.1 |