ENST00000334785.12:c.1145T>G
MANE Select
|
ENSP00000333938.7:p.Leu382Ter
|
|
ENST00000330010.12:c.953T>G
|
ENSP00000327363.8:p.Leu318Ter
|
|
ENST00000334785.11:c.1145T>G
|
ENSP00000333938.7:p.Leu382Ter
|
|
ENST00000342754.5:c.844T>G
|
|
|
ENST00000401035.7:c.953T>G
|
ENSP00000383814.3:p.Leu318Ter
|
|
ENST00000440324.5:c.1103T>G
|
ENSP00000411902.1:p.Leu368Ter
|
|
ENST00000464998.1:n.605T>G
|
|
|
ENST00000480732.2:n.719T>G
|
|
|
NM_001172309.1:c.953T>G
|
NP_001165780.1:p.Leu318Ter
|
|
NM_144573.3:c.1145T>G , LRG_442t1:c.1145T>G
|
NP_653174.3:p.Leu382Ter
|
|
XM_005271322.2:c.1145T>G
|
XP_005271379.1:p.Leu382Ter
|
|
XM_005271323.2:c.1103T>G
|
XP_005271380.1:p.Leu368Ter
|
|
XM_005271324.3:c.953T>G
|
XP_005271381.1:p.Leu318Ter
|
|
XM_005271325.2:c.1145T>G
|
XP_005271382.1:p.Leu382Ter
|
|
XM_005271326.2:c.911T>G
|
XP_005271383.1:p.Leu304Ter
|
|
XM_005271327.2:c.728T>G
|
XP_005271384.1:p.Leu243Ter
|
|
XM_005271322.4:c.1145T>G
|
XP_005271379.1:p.Leu382Ter
|
|
XM_005271323.4:c.1103T>G
|
XP_005271380.1:p.Leu368Ter
|
|
XM_005271324.5:c.953T>G
|
XP_005271381.1:p.Leu318Ter
|
|
XM_005271325.4:c.1145T>G
|
XP_005271382.1:p.Leu382Ter
|
|
XM_005271326.4:c.911T>G
|
XP_005271383.1:p.Leu304Ter
|
|
XM_005271327.4:c.728T>G
|
XP_005271384.1:p.Leu243Ter
|
|
NM_001172309.2:c.953T>G
|
NP_001165780.1:p.Leu318Ter
|
|
NM_144573.4:c.1145T>G
MANE Select
|
NP_653174.3:p.Leu382Ter
|
|