| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001265589.1 | 369 | Intron | NP_001252518.1 | ||
| NM_001265590.1 | 369 | Intron | NP_001252519.1 | ||
| NM_001265591.1 | 369 | Intron | NP_001252520.1 | ||
| NM_006054.3 | 369 | Intron | NP_006045.1 | ||
| NM_201428.2 | 369 | Intron | NP_958831.1 | ||
| NM_201429.2 | 369 | Intron | NP_958832.1 | ||
| NM_201430.2 | 369 | Intron | NP_958833.1 | ||
| XM_011544730.2 | 369 | Intron | XP_011543032.1 | ||
| XM_011544731.2 | 369 | Intron | XP_011543033.1 | ||
| XM_017017091.1 | 369 | Missense Mutation | CCA,CGA | P31R | XP_016872580.1 |
| XM_017017092.1 | 369 | Missense Mutation | CCA,CGA | P31R | XP_016872581.1 |