Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144980.3 | 1620 | Missense Mutation | AAC,AAG | N467K | NP_659417.2 |
XM_005266838.2 | 1620 | Missense Mutation | ACA,AGA | T486R | XP_005266895.1 |
XM_011535509.2 | 1620 | Missense Mutation | ACA,AGA | T521R | XP_011533811.1 |
XM_011535510.2 | 1620 | Missense Mutation | ACA,AGA | T501R | XP_011533812.1 |
XM_011535511.2 | 1620 | Missense Mutation | AAC,AAG | N502K | XP_011533813.1 |
XM_011535512.2 | 1620 | Missense Mutation | ACA,AGA | T382R | XP_011533814.1 |
XM_011535513.2 | 1620 | Missense Mutation | ACA,AGA | T382R | XP_011533815.1 |
XM_017010323.1 | 1620 | Intron | XP_016865812.1 | ||
XM_017010324.1 | 1620 | Missense Mutation | ACA,AGA | T382R | XP_016865813.1 |