| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001037162.1 | 393 | Missense Mutation | GGT,GTT | G21V | NP_001032239.1 |
| XM_011537076.2 | 393 | Missense Mutation | GGT,GTT | G273V | XP_011535378.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001220484.1 | 393 | Intron | NP_001207413.1 | ||
| NM_203309.2 | 393 | Intron | NP_976054.2 | ||
| XM_006720143.2 | 393 | Intron | XP_006720206.1 | ||
| XM_011536760.2 | 393 | Intron | XP_011535062.1 | ||
| XM_011536761.2 | 393 | Intron | XP_011535063.1 | ||
| XM_017021289.1 | 393 | Intron | XP_016876778.1 |