| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001319677.1 | 908 | Missense Mutation | CGC,TGC | R37C | NP_001306606.1 |
| NM_001319678.1 | 908 | Intron | NP_001306607.1 | ||
| NM_001319679.1 | 908 | Intron | NP_001306608.1 | ||
| NM_018056.3 | 908 | Missense Mutation | CGC,TGC | R164C | NP_060526.2 |
| XM_005270988.2 | 908 | Missense Mutation | CGC,TGC | R37C | XP_005271045.1 |
| XM_006710724.1 | 908 | Missense Mutation | CGC,TGC | R164C | XP_006710787.1 |
| XM_006710725.3 | 908 | Missense Mutation | CGC,TGC | R164C | XP_006710788.1 |
| XM_011541681.2 | 908 | Missense Mutation | CGC,TGC | R164C | XP_011539983.1 |
| XM_011541683.1 | 908 | Missense Mutation | CGC,TGC | R37C | XP_011539985.1 |
| XM_011541684.2 | 908 | Intron | XP_011539986.1 | ||
| XM_017001595.1 | 908 | Missense Mutation | CGC,TGC | R49C | XP_016857084.1 |