| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015017.4 | 3096 | Missense Mutation | ATT,GTT | I908V | NP_055832.3 |
| NM_201624.2 | 3096 | Missense Mutation | ATT,GTT | I877V | NP_963918.1 |
| NM_201626.2 | 3096 | Intron | NP_963920.1 | ||
| XM_005270648.1 | 3096 | Missense Mutation | ATT,GTT | I900V | XP_005270705.1 |
| XM_005270649.1 | 3096 | UTR 3 | XP_005270706.1 | ||
| XM_011541055.1 | 3096 | Missense Mutation | ATT,GTT | I809V | XP_011539357.1 |
| XM_011541056.2 | 3096 | Intron | XP_011539358.1 | ||
| XM_017000722.1 | 3096 | Missense Mutation | ATT,GTT | I869V | XP_016856211.1 |
| XM_017000723.1 | 3096 | UTR 3 | XP_016856212.1 | ||
| XM_017000724.1 | 3096 | UTR 3 | XP_016856213.1 | ||
| XM_017000725.1 | 3096 | Missense Mutation | ATT,GTT | I778V | XP_016856214.1 |
| XM_017000726.1 | 3096 | Missense Mutation | ATT,GTT | I770V | XP_016856215.1 |
| XM_017000727.1 | 3096 | Missense Mutation | ATT,GTT | I729V | XP_016856216.1 |
| XM_017000728.1 | 3096 | Missense Mutation | ATT,GTT | I729V | XP_016856217.1 |
| XM_017000729.1 | 3096 | UTR 3 | XP_016856218.1 |