| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144003.2 | 532 | Intron | NP_001137475.1 | ||
| NM_001144004.2 | 532 | Intron | NP_001137476.1 | ||
| NM_001144005.2 | 532 | Intron | NP_001137477.1 | ||
| NM_001144006.2 | 532 | Intron | NP_001137478.1 | ||
| NM_001144008.2 | 532 | Intron | NP_001137480.1 | ||
| NM_001144009.2 | 532 | Intron | NP_001137481.1 | ||
| NM_001144010.2 | 532 | Intron | NP_001137482.1 | ||
| NM_032539.4 | 532 | Intron | NP_115928.1 | ||
| XM_005262342.3 | 532 | UTR 3 | XP_005262399.1 | ||
| XM_005262343.3 | 532 | UTR 3 | XP_005262400.1 | ||
| XM_005262344.3 | 532 | UTR 3 | XP_005262401.1 | ||
| XM_005262345.3 | 532 | UTR 3 | XP_005262402.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004709.2 | 532 | Missense Mutation | ATG,ATT | M88I | NP_004700.1 |