Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012335.3 | 2945 | Missense Mutation | CCC,CTC | P960L | NP_036467.2 |
XM_011528024.1 | 2945 | Missense Mutation | CCC,CTC | P981L | XP_011526326.1 |
XM_011528025.1 | 2945 | Missense Mutation | CCC,CTC | P977L | XP_011526327.1 |
XM_011528026.1 | 2945 | Missense Mutation | CCC,CTC | P952L | XP_011526328.1 |
XM_011528027.1 | 2945 | Missense Mutation | CCC,CTC | P936L | XP_011526329.1 |
XM_011528028.2 | 2945 | Intron | XP_011526330.1 | ||
XM_017026821.1 | 2945 | Missense Mutation | CCC,CTC | P956L | XP_016882310.1 |