ENST00000215882.10:c.707T>A
MANE Select
|
ENSP00000215882.5:p.Phe236Tyr
|
|
ENST00000215882.9:c.707T>A
|
ENSP00000215882.5:p.Phe236Tyr
|
|
ENST00000451283.5:c.398T>A
|
ENSP00000401480.1:p.Phe133Tyr
|
|
ENST00000470922.5:n.849T>A
|
|
|
NM_001256534.1:c.728T>A
|
NP_001243463.1:p.Phe243Tyr
|
|
NM_001287387.1:c.398T>A
|
NP_001274316.1:p.Phe133Tyr
|
|
NM_005984.4:c.707T>A
|
NP_005975.1:p.Phe236Tyr
|
|
NR_046298.2:n.758T>A
|
|
|
NM_005984.5:c.707T>A
MANE Select
|
NP_005975.1:p.Phe236Tyr
|
|
NM_001256534.2:c.728T>A
|
NP_001243463.1:p.Phe243Tyr
|
|
NM_001287387.2:c.398T>A
|
NP_001274316.1:p.Phe133Tyr
|
|
NR_046298.3:n.631T>A
|
|
|