| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166049.1 | 982 | Intron | NP_001159521.1 | ||
| NM_001983.3 | 982 | Intron | NP_001974.1 | ||
| NM_202001.2 | 982 | Intron | NP_973730.1 | ||
| XM_005258634.1 | 982 | Intron | XP_005258691.1 | ||
| XM_005258635.2 | 982 | Intron | XP_005258692.1 | ||
| XM_005258636.4 | 982 | Intron | XP_005258693.1 | ||
| XM_005258637.1 | 982 | Intron | XP_005258694.1 | ||
| XM_011526610.2 | 982 | Intron | XP_011524912.1 | ||
| XM_017026459.1 | 982 | Intron | XP_016881948.1 | ||
| XM_017026460.1 | 982 | Intron | XP_016881949.1 | ||
| XM_017026461.1 | 982 | Intron | XP_016881950.1 | ||
| XM_017026462.1 | 982 | Intron | XP_016881951.1 | ||
| XM_017026463.1 | 982 | Intron | XP_016881952.1 | ||
| XM_017026464.1 | 982 | Intron | XP_016881953.1 | ||
| XM_017026465.1 | 982 | Intron | XP_016881954.1 | ||
| XM_017026466.1 | 982 | Intron | XP_016881955.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001114171.1 | 982 | Missense Mutation | AGG,AGT | R130S | NP_001107643.1 |
| NM_006732.2 | 982 | Missense Mutation | AGG,AGT | R130S | NP_006723.2 |
| XM_005258691.1 | 982 | Missense Mutation | AGG,AGT | R130S | XP_005258748.1 |