ENST00000359271.4:c.332C>T
MANE Select
|
ENSP00000352216.2:p.Ala111Val
|
|
ENST00000359271.3:c.332C>T
|
ENSP00000352216.2:p.Ala111Val
|
|
ENST00000611837.1:n.484C>T
|
|
|
NM_030777.3:c.332C>T
|
NP_110404.1:p.Ala111Val
|
|
XM_011529060.1:c.395C>T
|
XP_011527362.1:p.Ala132Val
|
|
XM_011529061.1:c.341C>T
|
XP_011527363.1:p.Ala114Val
|
|
XM_011529062.1:c.395C>T
|
XP_011527364.1:p.Ala132Val
|
|
XM_011529063.1:c.395C>T
|
XP_011527365.1:p.Ala132Val
|
|
XM_011529064.1:c.395C>T
|
XP_011527366.1:p.Ala132Val
|
|
XM_011529065.1:c.395C>T
|
XP_011527367.1:p.Ala132Val
|
|
XR_936641.1:n.531C>T
|
|
|
XM_011529060.2:c.395C>T
|
XP_011527362.1:p.Ala132Val
|
|
XM_011529061.2:c.341C>T
|
XP_011527363.1:p.Ala114Val
|
|
XM_011529062.2:c.395C>T
|
XP_011527364.1:p.Ala132Val
|
|
XM_011529063.2:c.395C>T
|
XP_011527365.1:p.Ala132Val
|
|
XM_011529064.2:c.395C>T
|
XP_011527366.1:p.Ala132Val
|
|
XM_011529065.2:c.395C>T
|
XP_011527367.1:p.Ala132Val
|
|
XM_017028087.2:c.332C>T
|
XP_016883576.1:p.Ala111Val
|
|
XR_936641.2:n.518C>T
|
|
|
NM_030777.4:c.332C>T
MANE Select
|
NP_110404.1:p.Ala111Val
|
|