ENST00000449082.3:c.3189G>C
MANE Select
|
ENSP00000390600.2:p.Glu1063Asp
|
|
ENST00000643924.1:c.3186G>C
|
ENSP00000495595.1:p.Glu1062Asp
|
|
ENST00000655275.1:c.3213G>C
|
ENSP00000499510.1:p.Glu1071Asp
|
|
ENST00000449082.2:c.3189G>C
|
ENSP00000390600.2:p.Glu1063Asp
|
|
NM_001293306.2:c.3186G>C
|
NP_001280235.2:p.Glu1062Asp
|
|
NM_001293307.2:c.2895G>C
|
NP_001280236.2:p.Glu965Asp
|
|
NM_006514.3:c.3189G>C
|
NP_006505.3:p.Glu1063Asp
|
|
XM_005265371.2:c.3198G>C
|
XP_005265428.1:p.Glu1066Asp
|
|
XM_011533993.1:c.3195G>C
|
XP_011532295.1:p.Glu1065Asp
|
|
XM_011533994.1:c.2904G>C
|
XP_011532296.1:p.Glu968Asp
|
|
XM_005265371.3:c.3198G>C
|
XP_005265428.1:p.Glu1066Asp
|
|
XM_011533993.2:c.3195G>C
|
XP_011532295.1:p.Glu1065Asp
|
|
XM_011533994.2:c.2904G>C
|
XP_011532296.1:p.Glu968Asp
|
|
NM_006514.4:c.3189G>C
MANE Select
|
NP_006505.4:p.Glu1063Asp
|
|