Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001242867.1 | 1202 | Intron | NP_001229796.1 | ||
NM_006737.3 | 1202 | Intron | NP_006728.2 | ||
XM_011526940.2 | 1202 | Missense Mutation | AAT,CAT | N349H | XP_011525242.1 |
XM_017026784.1 | 1202 | Intron | XP_016882273.1 |