ENST00000334785.12:c.1354T>G
MANE Select
|
ENSP00000333938.7:p.Phe452Val
|
|
ENST00000330010.12:c.1162T>G
|
ENSP00000327363.8:p.Phe388Val
|
|
ENST00000334785.11:c.1354T>G
|
ENSP00000333938.7:p.Phe452Val
|
|
ENST00000342754.5:c.1053T>G
|
|
|
ENST00000464998.1:n.814T>G
|
|
|
ENST00000480732.2:n.928T>G
|
|
|
NM_001172309.1:c.1162T>G
|
NP_001165780.1:p.Phe388Val
|
|
NM_144573.3:c.1354T>G , LRG_442t1:c.1354T>G
|
NP_653174.3:p.Phe452Val
|
|
XM_005271322.2:c.1354T>G
|
XP_005271379.1:p.Phe452Val
|
|
XM_005271323.2:c.1312T>G
|
XP_005271380.1:p.Phe438Val
|
|
XM_005271324.3:c.1162T>G
|
XP_005271381.1:p.Phe388Val
|
|
XM_005271325.2:c.1251+2446T>G
|
XP_005271382.1:n.1251+2446T>G
|
|
XM_005271326.2:c.1120T>G
|
XP_005271383.1:p.Phe374Val
|
|
XM_005271327.2:c.937T>G
|
XP_005271384.1:p.Phe313Val
|
|
XM_005271322.4:c.1354T>G
|
XP_005271379.1:p.Phe452Val
|
|
XM_005271323.4:c.1312T>G
|
XP_005271380.1:p.Phe438Val
|
|
XM_005271324.5:c.1162T>G
|
XP_005271381.1:p.Phe388Val
|
|
XM_005271325.4:c.1251+2446T>G
|
XP_005271382.1:n.1251+2446T>G
|
|
XM_005271326.4:c.1120T>G
|
XP_005271383.1:p.Phe374Val
|
|
XM_005271327.4:c.937T>G
|
XP_005271384.1:p.Phe313Val
|
|
NM_001172309.2:c.1162T>G
|
NP_001165780.1:p.Phe388Val
|
|
NM_144573.4:c.1354T>G
MANE Select
|
NP_653174.3:p.Phe452Val
|
|