ENST00000334785.12:c.1364T>G
MANE Select
|
ENSP00000333938.7:p.Ile455Ser
|
|
ENST00000330010.12:c.1172T>G
|
ENSP00000327363.8:p.Ile391Ser
|
|
ENST00000334785.11:c.1364T>G
|
ENSP00000333938.7:p.Ile455Ser
|
|
ENST00000342754.5:c.1063T>G
|
|
|
ENST00000464998.1:n.824T>G
|
|
|
ENST00000480732.2:n.938T>G
|
|
|
NM_001172309.1:c.1172T>G
|
NP_001165780.1:p.Ile391Ser
|
|
NM_144573.3:c.1364T>G , LRG_442t1:c.1364T>G
|
NP_653174.3:p.Ile455Ser
|
|
XM_005271322.2:c.1364T>G
|
XP_005271379.1:p.Ile455Ser
|
|
XM_005271323.2:c.1322T>G
|
XP_005271380.1:p.Ile441Ser
|
|
XM_005271324.3:c.1172T>G
|
XP_005271381.1:p.Ile391Ser
|
|
XM_005271325.2:c.1251+2456T>G
|
XP_005271382.1:n.1251+2456T>G
|
|
XM_005271326.2:c.1130T>G
|
XP_005271383.1:p.Ile377Ser
|
|
XM_005271327.2:c.947T>G
|
XP_005271384.1:p.Ile316Ser
|
|
XM_005271322.4:c.1364T>G
|
XP_005271379.1:p.Ile455Ser
|
|
XM_005271323.4:c.1322T>G
|
XP_005271380.1:p.Ile441Ser
|
|
XM_005271324.5:c.1172T>G
|
XP_005271381.1:p.Ile391Ser
|
|
XM_005271325.4:c.1251+2456T>G
|
XP_005271382.1:n.1251+2456T>G
|
|
XM_005271326.4:c.1130T>G
|
XP_005271383.1:p.Ile377Ser
|
|
XM_005271327.4:c.947T>G
|
XP_005271384.1:p.Ile316Ser
|
|
NM_001172309.2:c.1172T>G
|
NP_001165780.1:p.Ile391Ser
|
|
NM_144573.4:c.1364T>G
MANE Select
|
NP_653174.3:p.Ile455Ser
|
|