| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289119.1 | 477 | Missense Mutation | AGA,GGA | R102G | NP_001276048.1 |
| NM_001289120.1 | 477 | Missense Mutation | AGA,GGA | R102G | NP_001276049.1 |
| NM_001289121.1 | 477 | Missense Mutation | AGA,GGA | R102G | NP_001276050.1 |
| NM_032226.2 | 477 | Missense Mutation | AGA,GGA | R102G | NP_115602.2 |
| XM_005251608.4 | 477 | Missense Mutation | AGA,GGA | R102G | XP_005251665.1 |
| XM_005251612.2 | 477 | Missense Mutation | AGA,GGA | R102G | XP_005251669.1 |
| XM_011518050.1 | 477 | Missense Mutation | AGA,GGA | R102G | XP_011516352.1 |
| XM_011518051.2 | 477 | Intron | XP_011516353.1 | ||
| XM_017015197.1 | 477 | Missense Mutation | AGA,GGA | R102G | XP_016870686.1 |
| XM_017015198.1 | 477 | Missense Mutation | AGA,GGA | R102G | XP_016870687.1 |
| XM_017015199.1 | 477 | UTR 5 | XP_016870688.1 | ||
| XM_017015200.1 | 477 | UTR 5 | XP_016870689.1 | ||
| XM_017015201.1 | 477 | Intron | XP_016870690.1 |