| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164883.1 | 1282 | Intron | NP_001158355.1 | ||
| NM_001282597.2 | 1282 | Intron | NP_001269526.1 | ||
| NM_001282598.1 | 1282 | Intron | NP_001269527.1 | ||
| NM_001282599.1 | 1282 | Intron | NP_001269528.1 | ||
| NM_001282600.1 | 1282 | Intron | NP_001269529.1 | ||
| NM_001320810.1 | 1282 | Intron | NP_001307739.1 | ||
| NM_004389.3 | 1282 | Intron | NP_004380.2 | ||
| XM_011532555.2 | 1282 | Intron | XP_011530857.1 | ||
| XM_011532556.2 | 1282 | Intron | XP_011530858.1 | ||
| XM_011532557.2 | 1282 | Intron | XP_011530859.1 | ||
| XM_017003403.1 | 1282 | Intron | XP_016858892.1 | ||
| XM_017003404.1 | 1282 | Intron | XP_016858893.1 | ||
| XM_017003405.1 | 1282 | Intron | XP_016858894.1 | ||
| XM_017003406.1 | 1282 | Intron | XP_016858895.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178839.4 | 1282 | Missense Mutation | AGC,GGC | S338G | NP_849161.2 |
| XM_017003986.1 | 1282 | Missense Mutation | AGC,GGC | S338G | XP_016859475.1 |
| XM_017003987.1 | 1282 | Missense Mutation | AGC,GGC | S338G | XP_016859476.1 |