| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321307.1 | 4447 | Missense Mutation | GGT,TGT | G1201C | NP_001308236.1 |
| NM_002519.2 | 4447 | Missense Mutation | GGT,TGT | G1194C | NP_002510.2 |
| XM_011542854.2 | 4447 | Missense Mutation | GGT,TGT | G1203C | XP_011541156.1 |
| XM_017017802.1 | 4447 | Missense Mutation | GGT,TGT | G1135C | XP_016873291.1 |
| XM_017017803.1 | 4447 | Missense Mutation | GGT,TGT | G1135C | XP_016873292.1 |