ENST00000215882.10:c.665T>C
MANE Select
|
ENSP00000215882.5:p.Ile222Thr
|
|
ENST00000215882.9:c.665T>C
|
ENSP00000215882.5:p.Ile222Thr
|
|
ENST00000451283.5:c.356T>C
|
ENSP00000401480.1:p.Ile119Thr
|
|
ENST00000470922.5:n.807T>C
|
|
|
NM_001256534.1:c.686T>C
|
NP_001243463.1:p.Ile229Thr
|
|
NM_001287387.1:c.356T>C
|
NP_001274316.1:p.Ile119Thr
|
|
NM_005984.4:c.665T>C
|
NP_005975.1:p.Ile222Thr
|
|
NR_046298.2:n.716T>C
|
|
|
NM_005984.5:c.665T>C
MANE Select
|
NP_005975.1:p.Ile222Thr
|
|
NM_001256534.2:c.686T>C
|
NP_001243463.1:p.Ile229Thr
|
|
NM_001287387.2:c.356T>C
|
NP_001274316.1:p.Ile119Thr
|
|
NR_046298.3:n.589T>C
|
|
|