Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286490.1 | 1748 | Intron | NP_001273419.1 | ||
NM_001286491.1 | 1748 | Missense Mutation | CAT,CGT | H269R | NP_001273420.1 |
NM_001322949.1 | 1748 | Intron | NP_001309878.1 | ||
NM_001322950.1 | 1748 | Intron | NP_001309879.1 | ||
NM_001322951.1 | 1748 | Intron | NP_001309880.1 | ||
NM_032892.4 | 1748 | Missense Mutation | CAT,CGT | H503R | NP_116281.2 |
XM_005254730.3 | 1748 | Intron | XP_005254787.1 |