Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020979.4 | 143 | Missense Mutation | CCT,GCT | P16A | NP_066189.3 |
XM_005276975.4 | 143 | Missense Mutation | CCT,GCT | P16A | XP_005277032.1 |
XM_005276976.3 | 143 | Missense Mutation | CCT,GCT | P16A | XP_005277033.1 |
XM_005276977.4 | 143 | Intron | XP_005277034.1 | ||
XM_005276979.3 | 143 | Intron | XP_005277036.1 | ||
XM_011515740.2 | 143 | Intron | XP_011514042.1 | ||
XM_017011680.1 | 143 | Intron | XP_016867169.1 | ||
XM_017011681.1 | 143 | Intron | XP_016867170.1 |