ENST00000215882.10:c.736A=
MANE Select
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ENSP00000215882.5:p.Thr246=
|
|
ENST00000215882.9:c.736A=
|
ENSP00000215882.5:p.Thr246=
|
|
ENST00000451283.5:c.427A=
|
ENSP00000401480.1:p.Thr143=
|
|
ENST00000470922.5:n.878A=
|
|
|
NM_001256534.1:c.757A=
|
NP_001243463.1:p.Thr253=
|
|
NM_001287387.1:c.427A=
|
NP_001274316.1:p.Thr143=
|
|
NM_005984.4:c.736A=
|
NP_005975.1:p.Thr246=
|
|
NR_046298.2:n.787A=
|
|
|
NM_005984.5:c.736A=
MANE Select
|
NP_005975.1:p.Thr246=
|
|
NM_001256534.2:c.757A=
|
NP_001243463.1:p.Thr253=
|
|
NM_001287387.2:c.427A=
|
NP_001274316.1:p.Thr143=
|
|
NR_046298.3:n.660A=
|
|
|