Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001037304.1 | 614 | Intron | NP_001032381.1 | ||
NM_001037305.1 | 614 | Missense Mutation | CAT,CGT | H171R | NP_001032382.1 |
NM_014174.2 | 614 | Missense Mutation | CAT,CGT | H171R | NP_054893.1 |
NM_199297.1 | 614 | Intron | NP_954994.1 | ||
NM_199298.1 | 614 | Missense Mutation | CAT,CGT | H171R | NP_954995.1 |
XM_005271527.3 | 614 | Missense Mutation | CAT,CGT | H212R | XP_005271584.1 |
XM_005271528.3 | 614 | Intron | XP_005271585.1 |