ENST00000215882.10:c.827A>G
MANE Select
|
ENSP00000215882.5:p.Tyr276Cys
|
|
ENST00000215882.9:c.827A>G
|
ENSP00000215882.5:p.Tyr276Cys
|
|
ENST00000451283.5:c.518A>G
|
ENSP00000401480.1:p.Tyr173Cys
|
|
ENST00000470922.5:n.969A>G
|
|
|
NM_001256534.1:c.848A>G
|
NP_001243463.1:p.Tyr283Cys
|
|
NM_001287387.1:c.518A>G
|
NP_001274316.1:p.Tyr173Cys
|
|
NM_005984.4:c.827A>G
|
NP_005975.1:p.Tyr276Cys
|
|
NR_046298.2:n.878A>G
|
|
|
NM_005984.5:c.827A>G
MANE Select
|
NP_005975.1:p.Tyr276Cys
|
|
NM_001256534.2:c.848A>G
|
NP_001243463.1:p.Tyr283Cys
|
|
NM_001287387.2:c.518A>G
|
NP_001274316.1:p.Tyr173Cys
|
|
NR_046298.3:n.751A>G
|
|
|