ENST00000215882.10:c.660T>A
MANE Select
|
ENSP00000215882.5:p.Pro220=
|
|
ENST00000215882.9:c.660T>A
|
ENSP00000215882.5:p.Pro220=
|
|
ENST00000451283.5:c.351T>A
|
ENSP00000401480.1:p.Pro117=
|
|
ENST00000470922.5:n.802T>A
|
|
|
NM_001256534.1:c.681T>A
|
NP_001243463.1:p.Pro227=
|
|
NM_001287387.1:c.351T>A
|
NP_001274316.1:p.Pro117=
|
|
NM_005984.4:c.660T>A
|
NP_005975.1:p.Pro220=
|
|
NR_046298.2:n.711T>A
|
|
|
NM_005984.5:c.660T>A
MANE Select
|
NP_005975.1:p.Pro220=
|
|
NM_001256534.2:c.681T>A
|
NP_001243463.1:p.Pro227=
|
|
NM_001287387.2:c.351T>A
|
NP_001274316.1:p.Pro117=
|
|
NR_046298.3:n.584T>A
|
|
|