Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098537.2 | 4063 | Missense Mutation | CGC,TGC | R1231C | NP_001092007.2 |
NM_152286.4 | 4063 | Missense Mutation | CGC,TGC | R1206C | NP_689499.4 |
XM_006717102.1 | 4063 | Missense Mutation | CGC,TGC | R1232C | XP_006717165.1 |
XM_006717104.3 | 4063 | Missense Mutation | CGC,TGC | R1198C | XP_006717167.1 |
XM_011518664.2 | 4063 | Intron | XP_011516966.1 | ||
XM_017014709.1 | 4063 | Missense Mutation | CGC,TGC | R1198C | XP_016870198.1 |