| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032779.3 | 170 | Intron | NP_116168.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022492.4 | 170 | Missense Mutation | GGT,TGT | G36C | NP_071937.4 |
| XM_005264492.1 | 170 | Missense Mutation | GGT,TGT | G36C | XP_005264549.1 |
| XM_011533035.1 | 170 | Missense Mutation | GGT,TGT | G36C | XP_011531337.1 |
| XM_011533036.1 | 170 | Missense Mutation | GGT,TGT | G36C | XP_011531338.1 |
| XM_011533037.1 | 170 | Missense Mutation | GGT,TGT | G36C | XP_011531339.1 |
| XM_011533040.1 | 170 | UTR 5 | XP_011531342.1 | ||
| XM_017004706.1 | 170 | Missense Mutation | GGT,TGT | G36C | XP_016860195.1 |
| XM_017004707.1 | 170 | Missense Mutation | GGT,TGT | G36C | XP_016860196.1 |
| XM_017004708.1 | 170 | UTR 5 | XP_016860197.1 | ||
| XM_017004709.1 | 170 | Intron | XP_016860198.1 |