| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001167749.2 | 6128 | Missense Mutation | CGC,TGC | R1398C | NP_001161221.1 |
| NM_001297772.1 | 6128 | Missense Mutation | CGC,TGC | R1459C | NP_001284701.1 |
| NM_018417.5 | 6128 | Missense Mutation | CGC,TGC | R1551C | NP_060887.2 |
| XM_005245330.4 | 6128 | Intron | XP_005245387.1 | ||
| XM_006711449.3 | 6128 | Intron | XP_006711512.1 | ||
| XM_011509760.2 | 6128 | Missense Mutation | CGC,TGC | R1551C | XP_011508062.1 |
| XM_011509762.2 | 6128 | Missense Mutation | CGC,TGC | R1503C | XP_011508064.1 |
| XM_011509763.2 | 6128 | Missense Mutation | CGC,TGC | R1497C | XP_011508065.1 |
| XM_011509766.2 | 6128 | Intron | XP_011508068.1 | ||
| XM_017001778.1 | 6128 | Intron | XP_016857267.1 |