| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297590.1 | 2266 | Missense Mutation | CCC,TCC | P139S | NP_001284519.1 |
| NM_012099.1 | 2266 | Missense Mutation | CCC,TCC | P137S | NP_036231.1 |
| XM_017026180.1 | 2266 | UTR 5 | XP_016881669.1 | ||
| XM_017026181.1 | 2266 | UTR 5 | XP_016881670.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166049.1 | 2266 | UTR 3 | NP_001159521.1 | ||
| NM_001983.3 | 2266 | UTR 3 | NP_001974.1 | ||
| NM_202001.2 | 2266 | Intron | NP_973730.1 | ||
| XM_005258634.1 | 2266 | Intron | XP_005258691.1 | ||
| XM_005258635.2 | 2266 | Intron | XP_005258692.1 | ||
| XM_005258636.4 | 2266 | Intron | XP_005258693.1 | ||
| XM_005258637.1 | 2266 | Intron | XP_005258694.1 | ||
| XM_011526610.2 | 2266 | Intron | XP_011524912.1 | ||
| XM_017026459.1 | 2266 | Intron | XP_016881948.1 | ||
| XM_017026460.1 | 2266 | UTR 3 | XP_016881949.1 | ||
| XM_017026461.1 | 2266 | UTR 3 | XP_016881950.1 | ||
| XM_017026462.1 | 2266 | UTR 3 | XP_016881951.1 | ||
| XM_017026463.1 | 2266 | UTR 3 | XP_016881952.1 | ||
| XM_017026464.1 | 2266 | UTR 3 | XP_016881953.1 | ||
| XM_017026465.1 | 2266 | UTR 3 | XP_016881954.1 | ||
| XM_017026466.1 | 2266 | UTR 3 | XP_016881955.1 |