|
NM_004380.3:c.5128T>C
MANE Select
|
NP_004371.2:p.Cys1710Arg
|
|
ENST00000262367.10:c.5128T>C
MANE Select
|
ENSP00000262367.5:p.Cys1710Arg
|
|
NM_001079846.1:c.5014T>C
|
NP_001073315.1:p.Cys1672Arg
|
|
NM_004380.2:c.5128T>C
|
NP_004371.2:p.Cys1710Arg
|
|
ENST00000262367.9:c.5128T>C
|
ENSP00000262367.5:p.Cys1710Arg
|
|
ENST00000382070.7:c.5014T>C
|
ENSP00000371502.3:p.Cys1672Arg
|
|
ENST00000637492.1:c.15T>C
|
|
|
XM_005255124.3:c.5083T>C
|
XP_005255181.1:p.Cys1695Arg
|
|
XM_005255124.4:c.5083T>C
|
XP_005255181.1:p.Cys1695Arg
|
|
XM_005255125.3:c.4711T>C
|
XP_005255182.1:p.Cys1571Arg
|
|
XM_005255125.4:c.4711T>C
|
XP_005255182.1:p.Cys1571Arg
|
|
XM_006720848.2:c.4867T>C
|
XP_006720911.1:p.Cys1623Arg
|
|
XM_006720848.3:c.4867T>C
|
XP_006720911.1:p.Cys1623Arg
|
|
XM_011522380.1:c.5074T>C
|
XP_011520682.1:p.Cys1692Arg
|
|
XM_011522381.1:c.4375T>C
|
XP_011520683.1:p.Cys1459Arg
|
|
XM_011522381.2:c.4375T>C
|
XP_011520683.1:p.Cys1459Arg
|
|
XM_017022944.1:c.5122T>C
|
XP_016878433.1:p.Cys1708Arg
|