Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005778.3 | 441 | Missense Mutation | CAT,CCT | H89P | NP_005769.1 |
XM_006712917.1 | 441 | Missense Mutation | CAT,CCT | H89P | XP_006712980.1 |
XM_011533261.1 | 441 | Missense Mutation | CAT,CCT | H89P | XP_011531563.1 |
XM_011533262.1 | 441 | Missense Mutation | CAT,CCT | H89P | XP_011531564.1 |
XM_017005503.1 | 441 | Missense Mutation | CAT,CCT | H89P | XP_016860992.1 |
XM_017005504.1 | 441 | Missense Mutation | CAT,CCT | H89P | XP_016860993.1 |
XM_017005505.1 | 441 | UTR 5 | XP_016860994.1 | ||
XM_017005506.1 | 441 | UTR 5 | XP_016860995.1 | ||
XM_017005507.1 | 441 | UTR 5 | XP_016860996.1 |