Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015030.1 | 6268 | Missense Mutation | CGC,CTC | R2991L | NP_055845.1 |
XM_005248090.4 | 6268 | Missense Mutation | CGC,CTC | R3006L | XP_005248147.1 |
XM_005248093.4 | 6268 | Missense Mutation | CGC,CTC | R2022L | XP_005248150.1 |
XM_011513680.2 | 6268 | Missense Mutation | CGC,CTC | R3005L | XP_011511982.1 |
XM_011513681.2 | 6268 | Missense Mutation | CGC,CTC | R3000L | XP_011511983.1 |
XM_011513682.2 | 6268 | Missense Mutation | CGC,CTC | R2985L | XP_011511984.1 |
XM_011513683.2 | 6268 | Missense Mutation | CGC,CTC | R3006L | XP_011511985.1 |
XM_011513684.2 | 6268 | Missense Mutation | CGC,CTC | R2022L | XP_011511986.1 |
XM_011513685.2 | 6268 | Intron | XP_011511987.1 | ||
XM_017008046.1 | 6268 | Missense Mutation | CGC,CTC | R2991L | XP_016863535.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_175619.2 | 6268 | Intron | NP_783318.1 |