ENST00000215882.10:c.627C>G
MANE Select
|
ENSP00000215882.5:p.Tyr209Ter
|
|
ENST00000215882.9:c.627C>G
|
ENSP00000215882.5:p.Tyr209Ter
|
|
ENST00000451283.5:c.318C>G
|
ENSP00000401480.1:p.Tyr106Ter
|
|
ENST00000461267.1:n.773C>G
|
|
|
ENST00000470922.5:n.769C>G
|
|
|
NM_001256534.1:c.648C>G
|
NP_001243463.1:p.Tyr216Ter
|
|
NM_001287387.1:c.318C>G
|
NP_001274316.1:p.Tyr106Ter
|
|
NM_005984.4:c.627C>G
|
NP_005975.1:p.Tyr209Ter
|
|
NR_046298.2:n.678C>G
|
|
|
NM_005984.5:c.627C>G
MANE Select
|
NP_005975.1:p.Tyr209Ter
|
|
NM_001256534.2:c.648C>G
|
NP_001243463.1:p.Tyr216Ter
|
|
NM_001287387.2:c.318C>G
|
NP_001274316.1:p.Tyr106Ter
|
|
NR_046298.3:n.551C>G
|
|
|