| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171740.2 | 697 | Intron | NP_001165211.1 | ||
| NM_001171741.2 | 697 | Intron | NP_001165212.1 | ||
| NM_001171743.2 | 697 | Intron | NP_001165214.2 | ||
| NM_016210.4 | 697 | Intron | NP_057294.2 | ||
| XM_011533781.2 | 697 | Intron | XP_011532083.1 | ||
| XM_011533782.2 | 697 | Intron | XP_011532084.1 | ||
| XM_011533783.2 | 697 | Intron | XP_011532085.1 | ||
| XM_011533784.2 | 697 | Intron | XP_011532086.1 | ||
| XM_011533785.2 | 697 | Intron | XP_011532087.1 | ||
| XM_011533788.1 | 697 | Intron | XP_011532090.1 | ||
| XM_011533789.1 | 697 | Intron | XP_011532091.1 | ||
| XM_011533790.1 | 697 | Intron | XP_011532092.1 | ||
| XM_017006545.1 | 697 | Intron | XP_016862034.1 | ||
| XM_017006546.1 | 697 | Intron | XP_016862035.1 | ||
| XM_017006547.1 | 697 | Intron | XP_016862036.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317851.1 | 697 | Missense Mutation | CCT,TCT | P34S | NP_001304780.1 |
| NM_016173.4 | 697 | Missense Mutation | CCT,TCT | P34S | NP_057257.1 |
| XM_005265218.3 | 697 | Missense Mutation | CCT,TCT | P34S | XP_005265275.1 |
| XM_011533806.2 | 697 | Missense Mutation | CCT,TCT | P34S | XP_011532108.1 |
| XM_011533807.1 | 697 | Missense Mutation | CCT,TCT | P34S | XP_011532109.1 |
| XM_011533808.1 | 697 | Missense Mutation | CCT,TCT | P34S | XP_011532110.1 |
| XM_011533809.2 | 697 | Missense Mutation | CCT,TCT | P34S | XP_011532111.1 |
| XM_011533810.2 | 697 | Missense Mutation | CCT,TCT | P34S | XP_011532112.1 |
| XM_011533812.2 | 697 | Missense Mutation | CCT,TCT | P34S | XP_011532114.1 |
| XM_011533813.2 | 697 | UTR 5 | XP_011532115.1 | ||
| XM_011533814.2 | 697 | UTR 5 | XP_011532116.1 |