| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010853.2 | 1178 | Intron | NP_001010853.1 | ||
| XM_005248661.2 | 1178 | Intron | XP_005248718.1 | ||
| XM_005248662.4 | 1178 | Intron | XP_005248719.1 | ||
| XM_011535481.2 | 1178 | Intron | XP_011533783.1 | ||
| XM_017010289.1 | 1178 | Intron | XP_016865778.1 | ||
| XM_017010290.1 | 1178 | Intron | XP_016865779.1 | ||
| XM_017010291.1 | 1178 | Intron | XP_016865780.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_080743.4 | 1178 | Missense Mutation | CAT,CGT | H243R | NP_542781.3 |
| XM_006715348.2 | 1178 | Missense Mutation | CAT,CGT | H148R | XP_006715411.1 |
| XM_011535483.2 | 1178 | Missense Mutation | CAT,CGT | H228R | XP_011533785.1 |
| XM_011535484.1 | 1178 | Missense Mutation | CAT,CGT | H148R | XP_011533786.1 |
| XM_017010292.1 | 1178 | Missense Mutation | CAT,CGT | H243R | XP_016865781.1 |
| XM_017010293.1 | 1178 | Missense Mutation | CAT,CGT | H148R | XP_016865782.1 |