|
NM_005984.5:c.821C>T
MANE Select
|
NP_005975.1:p.Ala274Val
|
|
ENST00000215882.10:c.821C>T
MANE Select
|
ENSP00000215882.5:p.Ala274Val
|
|
NM_001256534.1:c.842C>T
|
NP_001243463.1:p.Ala281Val
|
|
NM_001256534.2:c.842C>T
|
NP_001243463.1:p.Ala281Val
|
|
NM_001287387.1:c.512C>T
|
NP_001274316.1:p.Ala171Val
|
|
NM_001287387.2:c.512C>T
|
NP_001274316.1:p.Ala171Val
|
|
NM_005984.4:c.821C>T
|
NP_005975.1:p.Ala274Val
|
|
NR_046298.2:n.872C>T
|
|
|
NR_046298.3:n.745C>T
|
|
|
ENST00000215882.9:c.821C>T
|
ENSP00000215882.5:p.Ala274Val
|
|
ENST00000451283.5:c.512C>T
|
ENSP00000401480.1:p.Ala171Val
|
|
ENST00000470922.5:n.963C>T
|
|