ENST00000215882.10:c.797T>A
MANE Select
|
ENSP00000215882.5:p.Ile266Asn
|
|
ENST00000215882.9:c.797T>A
|
ENSP00000215882.5:p.Ile266Asn
|
|
ENST00000451283.5:c.488T>A
|
ENSP00000401480.1:p.Ile163Asn
|
|
ENST00000470922.5:n.939T>A
|
|
|
NM_001256534.1:c.818T>A
|
NP_001243463.1:p.Ile273Asn
|
|
NM_001287387.1:c.488T>A
|
NP_001274316.1:p.Ile163Asn
|
|
NM_005984.4:c.797T>A
|
NP_005975.1:p.Ile266Asn
|
|
NR_046298.2:n.848T>A
|
|
|
NM_005984.5:c.797T>A
MANE Select
|
NP_005975.1:p.Ile266Asn
|
|
NM_001256534.2:c.818T>A
|
NP_001243463.1:p.Ile273Asn
|
|
NM_001287387.2:c.488T>A
|
NP_001274316.1:p.Ile163Asn
|
|
NR_046298.3:n.721T>A
|
|
|