| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020859.3 | 846 | Missense Mutation | CCG,CTG | P32L | NP_065910.3 |
| XM_005263163.4 | 846 | Intron | XP_005263220.1 | ||
| XM_005263164.4 | 846 | Intron | XP_005263221.1 | ||
| XM_005263165.4 | 846 | Intron | XP_005263222.1 | ||
| XM_006714282.3 | 846 | Intron | XP_006714345.1 | ||
| XM_011532157.2 | 846 | Intron | XP_011530459.2 | ||
| XM_011532158.2 | 846 | Missense Mutation | CCG,CTG | P32L | XP_011530460.1 |
| XM_011532159.1 | 846 | Missense Mutation | CCG,CTG | P32L | XP_011530461.1 |
| XM_011532160.1 | 846 | Intron | XP_011530462.1 | ||
| XM_011532161.2 | 846 | Intron | XP_011530463.1 | ||
| XM_017008488.1 | 846 | Intron | XP_016863977.1 | ||
| XM_017008489.1 | 846 | Intron | XP_016863978.1 |