ENST00000262367.10:c.7141G>C
MANE Select
|
ENSP00000262367.5:p.Gly2381Arg
|
|
ENST00000262367.9:c.7141G>C
|
ENSP00000262367.5:p.Gly2381Arg
|
|
ENST00000382070.7:c.7027G>C
|
ENSP00000371502.3:p.Gly2343Arg
|
|
NM_001079846.1:c.7027G>C
|
NP_001073315.1:p.Gly2343Arg
|
|
NM_004380.2:c.7141G>C
|
NP_004371.2:p.Gly2381Arg
|
|
XM_005255124.3:c.7096G>C
|
XP_005255181.1:p.Gly2366Arg
|
|
XM_005255125.3:c.6724G>C
|
XP_005255182.1:p.Gly2242Arg
|
|
XM_006720848.2:c.6880G>C
|
XP_006720911.1:p.Gly2294Arg
|
|
XM_011522380.1:c.7087G>C
|
XP_011520682.1:p.Gly2363Arg
|
|
XM_011522381.1:c.6388G>C
|
XP_011520683.1:p.Gly2130Arg
|
|
XM_005255124.4:c.7096G>C
|
XP_005255181.1:p.Gly2366Arg
|
|
XM_005255125.4:c.6724G>C
|
XP_005255182.1:p.Gly2242Arg
|
|
XM_006720848.3:c.6880G>C
|
XP_006720911.1:p.Gly2294Arg
|
|
XM_011522381.2:c.6388G>C
|
XP_011520683.1:p.Gly2130Arg
|
|
XM_017022944.1:c.7135G>C
|
XP_016878433.1:p.Gly2379Arg
|
|
NM_004380.3:c.7141G>C
MANE Select
|
NP_004371.2:p.Gly2381Arg
|
|