| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_198578.3 | 262 | Missense Mutation | GGC,TGC | G9C | NP_940980.3 |
| XM_005268629.3 | 262 | Missense Mutation | GGC,TGC | G9C | XP_005268686.1 |
| XM_011537877.2 | 262 | Missense Mutation | GGC,TGC | G9C | XP_011536179.1 |
| XM_011537881.2 | 262 | Missense Mutation | GGC,TGC | G9C | XP_011536183.1 |
| XM_011537882.2 | 262 | Missense Mutation | GGC,TGC | G9C | XP_011536184.1 |
| XM_017018786.1 | 262 | Missense Mutation | GGC,TGC | G9C | XP_016874275.1 |
| XM_017018787.1 | 262 | Intron | XP_016874276.1 | ||
| XM_017018788.1 | 262 | Intron | XP_016874277.1 | ||
| XM_017018789.1 | 262 | Missense Mutation | GGC,TGC | G9C | XP_016874278.1 |