| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172655.1 | 1996 | Intron | NP_001166126.1 | ||
| NM_018260.2 | 1996 | Intron | NP_060730.2 | ||
| XM_011527092.1 | 1996 | Intron | XP_011525394.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001105549.1 | 1996 | Intron | NP_001099019.1 | ||
| NM_001105550.1 | 1996 | Intron | NP_001099020.1 | ||
| NM_001105551.1 | 1996 | Intron | NP_001099021.1 | ||
| NM_001105552.1 | 1996 | Intron | NP_001099022.1 | ||
| NM_001277945.1 | 1996 | Missense Mutation | CGC,CTC | R472L | NP_001264874.1 |
| NM_001277946.1 | 1996 | Missense Mutation | CGC,CTC | R472L | NP_001264875.1 |
| NM_001277947.1 | 1996 | Missense Mutation | CGC,CTC | R472L | NP_001264876.1 |
| NM_001277948.1 | 1996 | Missense Mutation | CGC,CTC | R472L | NP_001264877.1 |
| NM_001277949.1 | 1996 | Missense Mutation | CGC,CTC | R472L | NP_001264878.1 |
| NM_001277951.1 | 1996 | Intron | NP_001264880.1 | ||
| NM_001277952.1 | 1996 | Intron | NP_001264881.1 | ||
| NM_018300.3 | 1996 | Intron | NP_060770.3 | ||
| XM_017026951.1 | 1996 | Missense Mutation | CGC,CTC | R472L | XP_016882440.1 |