| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014831.2 | 9600 | Missense Mutation | GGC,GTC | G2808V | NP_055646.2 |
| XM_006713432.3 | 9600 | Missense Mutation | GGC,GTC | G2852V | XP_006713495.1 |
| XM_011534289.2 | 9600 | Missense Mutation | GGC,GTC | G2853V | XP_011532591.1 |
| XM_017007570.1 | 9600 | Missense Mutation | GGC,GTC | G2819V | XP_016863059.1 |
| XM_017007571.1 | 9600 | Missense Mutation | GGC,GTC | G2876V | XP_016863060.1 |
| XM_017007572.1 | 9600 | Missense Mutation | GGC,GTC | G2844V | XP_016863061.1 |
| XM_017007573.1 | 9600 | Intron | XP_016863062.1 |