| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_019855.4 | 2232 | Intron | NP_062829.1 | ||
| XM_017026992.1 | 2232 | Missense Mutation | ATG,GTG | M51V | XP_016882481.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159322.1 | 2232 | UTR 3 | NP_001152794.1 | ||
| NM_001159323.1 | 2232 | UTR 3 | NP_001152795.1 | ||
| NM_003706.2 | 2232 | UTR 3 | NP_003697.2 | ||
| XM_011527431.2 | 2232 | UTR 3 | XP_011525733.1 | ||
| XM_011527432.2 | 2232 | Intron | XP_011525734.1 | ||
| XM_011527433.2 | 2232 | Intron | XP_011525735.1 | ||
| XM_017027411.1 | 2232 | UTR 3 | XP_016882900.1 | ||
| XM_017027412.1 | 2232 | UTR 3 | XP_016882901.1 | ||
| XM_017027413.1 | 2232 | UTR 3 | XP_016882902.1 | ||
| XM_017027414.1 | 2232 | Intron | XP_016882903.1 |