ENST00000449082.3:c.3124C>G
MANE Select
|
ENSP00000390600.2:p.His1042Asp
|
|
ENST00000643924.1:c.3121C>G
|
ENSP00000495595.1:p.His1041Asp
|
|
ENST00000655275.1:c.3148C>G
|
ENSP00000499510.1:p.His1050Asp
|
|
ENST00000449082.2:c.3124C>G
|
ENSP00000390600.2:p.His1042Asp
|
|
NM_001293306.2:c.3121C>G
|
NP_001280235.2:p.His1041Asp
|
|
NM_001293307.2:c.2830C>G
|
NP_001280236.2:p.His944Asp
|
|
NM_006514.3:c.3124C>G
|
NP_006505.3:p.His1042Asp
|
|
XM_005265371.2:c.3133C>G
|
XP_005265428.1:p.His1045Asp
|
|
XM_011533993.1:c.3130C>G
|
XP_011532295.1:p.His1044Asp
|
|
XM_011533994.1:c.2839C>G
|
XP_011532296.1:p.His947Asp
|
|
XM_005265371.3:c.3133C>G
|
XP_005265428.1:p.His1045Asp
|
|
XM_011533993.2:c.3130C>G
|
XP_011532295.1:p.His1044Asp
|
|
XM_011533994.2:c.2839C>G
|
XP_011532296.1:p.His947Asp
|
|
NM_006514.4:c.3124C>G
MANE Select
|
NP_006505.4:p.His1042Asp
|
|