Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198580.2 | 272 | Missense Mutation | CCG,TCG | P79S | NP_940982.1 |
XM_011528000.1 | 272 | Missense Mutation | CCG,TCG | P79S | XP_011526302.1 |
XM_011528001.2 | 272 | Missense Mutation | CCG,TCG | P79S | XP_011526303.1 |
XM_011528002.2 | 272 | Missense Mutation | CCG,TCG | P79S | XP_011526304.1 |
XM_011528003.2 | 272 | Missense Mutation | CCG,TCG | P79S | XP_011526305.1 |
XM_017026781.1 | 272 | Missense Mutation | CCG,TCG | P79S | XP_016882270.1 |