| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195822.1 | 716 | Intron | NP_001182751.1 | ||
| NM_032303.4 | 716 | Missense Mutation | CCA,CGA | P154R | NP_115679.2 |
| XM_011519091.2 | 716 | Missense Mutation | CCA,CGA | P154R | XP_011517393.1 |
| XM_017015203.1 | 716 | Intron | XP_016870692.1 | ||
| XM_017015204.1 | 716 | Intron | XP_016870693.1 | ||
| XM_017015205.1 | 716 | Intron | XP_016870694.1 |