ENST00000215882.10:c.679G>T
MANE Select
|
ENSP00000215882.5:p.Gly227Ter
|
|
ENST00000215882.9:c.679G>T
|
ENSP00000215882.5:p.Gly227Ter
|
|
ENST00000451283.5:c.370G>T
|
ENSP00000401480.1:p.Gly124Ter
|
|
ENST00000470922.5:n.821G>T
|
|
|
NM_001256534.1:c.700G>T
|
NP_001243463.1:p.Gly234Ter
|
|
NM_001287387.1:c.370G>T
|
NP_001274316.1:p.Gly124Ter
|
|
NM_005984.4:c.679G>T
|
NP_005975.1:p.Gly227Ter
|
|
NR_046298.2:n.730G>T
|
|
|
NM_005984.5:c.679G>T
MANE Select
|
NP_005975.1:p.Gly227Ter
|
|
NM_001256534.2:c.700G>T
|
NP_001243463.1:p.Gly234Ter
|
|
NM_001287387.2:c.370G>T
|
NP_001274316.1:p.Gly124Ter
|
|
NR_046298.3:n.603G>T
|
|
|