ENST00000215882.10:c.931G>T
MANE Select
|
ENSP00000215882.5:p.Asp311Tyr
|
|
ENST00000215882.9:c.931G>T
|
ENSP00000215882.5:p.Asp311Tyr
|
|
ENST00000451283.5:c.622G>T
|
ENSP00000401480.1:p.Asp208Tyr
|
|
ENST00000470922.5:n.1073G>T
|
|
|
NM_001256534.1:c.952G>T
|
NP_001243463.1:p.Asp318Tyr
|
|
NM_001287387.1:c.622G>T
|
NP_001274316.1:p.Asp208Tyr
|
|
NM_005984.4:c.931G>T
|
NP_005975.1:p.Asp311Tyr
|
|
NR_046298.2:n.982G>T
|
|
|
NM_005984.5:c.931G>T
MANE Select
|
NP_005975.1:p.Asp311Tyr
|
|
NM_001256534.2:c.952G>T
|
NP_001243463.1:p.Asp318Tyr
|
|
NM_001287387.2:c.622G>T
|
NP_001274316.1:p.Asp208Tyr
|
|
NR_046298.3:n.855G>T
|
|
|