ENST00000219097.7:c.365A>T
MANE Select
|
ENSP00000219097.2:p.Glu122Val
|
|
ENST00000219097.6:c.365A>T
|
ENSP00000219097.2:p.Glu122Val
|
|
ENST00000563306.5:n.448A>T
|
|
|
ENST00000563599.5:c.*187A>T
|
ENSP00000454299.1:n.*187A>T
|
|
ENST00000566860.1:c.218A>T
|
ENSP00000456981.1:p.Glu73Val
|
|
ENST00000568364.6:c.365A>T
|
ENSP00000457282.2:p.Glu122Val
|
|
ENST00000569239.5:n.412A>T
|
|
|
ENST00000570260.2:n.364A>T
|
|
|
NM_014321.3:c.365A>T
|
NP_055136.1:p.Glu122Val
|
|
NR_037620.1:n.484A>T
|
|
|
XM_011522978.1:c.365A>T
|
XP_011521280.1:p.Glu122Val
|
|
XM_011522978.3:c.365A>T
|
XP_011521280.1:p.Glu122Val
|
|
NM_014321.4:c.365A>T
MANE Select
|
NP_055136.1:p.Glu122Val
|
|
NR_037620.2:n.471A>T
|
|
|