ENST00000334785.12:c.1625T>G
MANE Select
|
ENSP00000333938.7:p.Phe542Cys
|
|
ENST00000330010.12:c.1433T>G
|
ENSP00000327363.8:p.Phe478Cys
|
|
ENST00000334785.11:c.1625T>G
|
ENSP00000333938.7:p.Phe542Cys
|
|
ENST00000342754.5:c.1324T>G
|
|
|
ENST00000470735.1:n.464T>G
|
|
|
ENST00000480732.2:n.1199T>G
|
|
|
NM_001172309.1:c.1433T>G
|
NP_001165780.1:p.Phe478Cys
|
|
NM_144573.3:c.1625T>G , LRG_442t1:c.1625T>G
|
NP_653174.3:p.Phe542Cys
|
|
XM_005271322.2:c.1625T>G
|
XP_005271379.1:p.Phe542Cys
|
|
XM_005271323.2:c.1583T>G
|
XP_005271380.1:p.Phe528Cys
|
|
XM_005271324.3:c.1433T>G
|
XP_005271381.1:p.Phe478Cys
|
|
XM_005271325.2:c.1403T>G
|
XP_005271382.1:p.Phe468Cys
|
|
XM_005271326.2:c.1391T>G
|
XP_005271383.1:p.Phe464Cys
|
|
XM_005271327.2:c.1208T>G
|
XP_005271384.1:p.Phe403Cys
|
|
XM_005271322.4:c.1625T>G
|
XP_005271379.1:p.Phe542Cys
|
|
XM_005271323.4:c.1583T>G
|
XP_005271380.1:p.Phe528Cys
|
|
XM_005271324.5:c.1433T>G
|
XP_005271381.1:p.Phe478Cys
|
|
XM_005271325.4:c.1403T>G
|
XP_005271382.1:p.Phe468Cys
|
|
XM_005271326.4:c.1391T>G
|
XP_005271383.1:p.Phe464Cys
|
|
XM_005271327.4:c.1208T>G
|
XP_005271384.1:p.Phe403Cys
|
|
NM_001172309.2:c.1433T>G
|
NP_001165780.1:p.Phe478Cys
|
|
NM_144573.4:c.1625T>G
MANE Select
|
NP_653174.3:p.Phe542Cys
|
|