ENST00000215882.10:c.541T>A
MANE Select
|
ENSP00000215882.5:p.Tyr181Asn
|
|
ENST00000215882.9:c.541T>A
|
ENSP00000215882.5:p.Tyr181Asn
|
|
ENST00000451283.5:c.232T>A
|
ENSP00000401480.1:p.Tyr78Asn
|
|
ENST00000461267.1:n.687T>A
|
|
|
ENST00000470922.5:n.683T>A
|
|
|
NM_001256534.1:c.562T>A
|
NP_001243463.1:p.Tyr188Asn
|
|
NM_001287387.1:c.232T>A
|
NP_001274316.1:p.Tyr78Asn
|
|
NM_005984.4:c.541T>A
|
NP_005975.1:p.Tyr181Asn
|
|
NR_046298.2:n.592T>A
|
|
|
NM_005984.5:c.541T>A
MANE Select
|
NP_005975.1:p.Tyr181Asn
|
|
NM_001256534.2:c.562T>A
|
NP_001243463.1:p.Tyr188Asn
|
|
NM_001287387.2:c.232T>A
|
NP_001274316.1:p.Tyr78Asn
|
|
NR_046298.3:n.465T>A
|
|
|