| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320047.1 | 121 | Intron | NP_001306976.1 | ||
| NM_001320048.1 | 121 | UTR 5 | NP_001306977.1 | ||
| NM_001320050.1 | 121 | Missense Mutation | CCA,CTA | P8L | NP_001306979.1 |
| NM_001320051.1 | 121 | Intron | NP_001306980.1 | ||
| NM_018186.3 | 121 | Intron | NP_060656.2 | ||
| XM_005245317.4 | 121 | Missense Mutation | CCA,CTA | P8L | XP_005245374.1 |
| XM_011509735.2 | 121 | Intron | XP_011508037.1 | ||
| XM_017001722.1 | 121 | Missense Mutation | CCA,CTA | P8L | XP_016857211.1 |
| XM_017001723.1 | 121 | Missense Mutation | CCA,CTA | P8L | XP_016857212.1 |
| XM_017001724.1 | 121 | Intron | XP_016857213.1 | ||
| XM_017001725.1 | 121 | Intron | XP_016857214.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320199.1 | 121 | Intron | NP_001307128.1 | ||
| NM_001320201.1 | 121 | Intron | NP_001307130.1 | ||
| NM_033418.3 | 121 | Intron | NP_219486.1 | ||
| XM_006711627.3 | 121 | Intron | XP_006711690.1 |