| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001207067.1 | 725 | Missense Mutation | ATC,ATG | I90M | NP_001193996.1 |
| NM_001207069.1 | 725 | Intron | NP_001193998.1 | ||
| NM_001321688.1 | 725 | Intron | NP_001308617.1 | ||
| NM_001321690.1 | 725 | Intron | NP_001308619.1 | ||
| NM_001321691.1 | 725 | Intron | NP_001308620.1 | ||
| NM_001321693.1 | 725 | Intron | NP_001308622.1 | ||
| NM_001321694.1 | 725 | Intron | NP_001308623.1 | ||
| NM_014670.3 | 725 | Missense Mutation | ATC,ATG | I90M | NP_055485.2 |
| XM_017005393.1 | 725 | Intron | XP_016860882.1 |