Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006143.2 | 3912 | Missense Mutation | CCC,CGC | P405R | NP_006134.1 |
XM_011520623.2 | 3912 | Missense Mutation | CCC,CGC | P424R | XP_011518925.1 |
XM_011520624.2 | 3912 | Missense Mutation | CCC,CGC | P424R | XP_011518926.1 |
XM_011520625.2 | 3912 | Missense Mutation | CCC,CGC | P405R | XP_011518927.1 |
XM_017019212.1 | 3912 | Missense Mutation | CCC,CGC | P424R | XP_016874701.1 |
XM_017019213.1 | 3912 | Missense Mutation | CCC,CGC | P424R | XP_016874702.1 |
XM_017019214.1 | 3912 | Missense Mutation | CCC,CGC | P424R | XP_016874703.1 |
XM_017019215.1 | 3912 | Missense Mutation | CCC,CGC | P424R | XP_016874704.1 |
XM_017019216.1 | 3912 | Missense Mutation | CCC,CGC | P405R | XP_016874705.1 |