ENST00000449082.3:c.3316G>C
MANE Select
|
ENSP00000390600.2:p.Asp1106His
|
|
ENST00000643924.1:c.3313G>C
|
ENSP00000495595.1:p.Asp1105His
|
|
ENST00000655275.1:c.3340G>C
|
ENSP00000499510.1:p.Asp1114His
|
|
ENST00000449082.2:c.3316G>C
|
ENSP00000390600.2:p.Asp1106His
|
|
NM_001293306.2:c.3313G>C
|
NP_001280235.2:p.Asp1105His
|
|
NM_001293307.2:c.3022G>C
|
NP_001280236.2:p.Asp1008His
|
|
NM_006514.3:c.3316G>C
|
NP_006505.3:p.Asp1106His
|
|
XM_005265371.2:c.3325G>C
|
XP_005265428.1:p.Asp1109His
|
|
XM_011533993.1:c.3322G>C
|
XP_011532295.1:p.Asp1108His
|
|
XM_011533994.1:c.3031G>C
|
XP_011532296.1:p.Asp1011His
|
|
XM_005265371.3:c.3325G>C
|
XP_005265428.1:p.Asp1109His
|
|
XM_011533993.2:c.3322G>C
|
XP_011532295.1:p.Asp1108His
|
|
XM_011533994.2:c.3031G>C
|
XP_011532296.1:p.Asp1011His
|
|
NM_006514.4:c.3316G>C
MANE Select
|
NP_006505.4:p.Asp1106His
|
|