ENST00000328300.11:c.4444T>C
MANE Select
|
ENSP00000331902.7:p.Cys1482Arg
|
|
ENST00000361603.7:c.4426T>C
|
ENSP00000354505.2:p.Cys1476Arg
|
|
ENST00000510690.2:n.938T>C
|
|
|
ENST00000328300.10:c.4444T>C
|
ENSP00000331902.6:p.Cys1482Arg
|
|
ENST00000361603.6:c.4426T>C
|
ENSP00000354505.2:p.Cys1476Arg
|
|
ENST00000515658.1:c.240T>C
|
|
|
NM_000495.4:c.4426T>C
|
NP_000486.1:p.Cys1476Arg
|
|
NM_033380.2:c.4444T>C
|
NP_203699.1:p.Cys1482Arg
|
|
XM_005262070.2:c.4435T>C
|
XP_005262127.1:p.Cys1479Arg
|
|
XM_006724616.2:c.4444T>C
|
XP_006724679.1:p.Cys1482Arg
|
|
XM_011530849.1:c.4120T>C
|
XP_011529151.1:p.Cys1374Arg
|
|
XM_011530851.1:c.2017T>C
|
XP_011529153.1:p.Cys673Arg
|
|
XM_011530849.2:c.4459T>C
|
XP_011529151.2:p.Cys1487Arg
|
|
XM_017029259.2:c.4450T>C
|
XP_016884748.1:p.Cys1484Arg
|
|
XM_017029260.1:c.4441T>C
|
XP_016884749.1:p.Cys1481Arg
|
|
XM_017029263.2:c.2779T>C
|
XP_016884752.1:p.Cys927Arg
|
|
NM_000495.5:c.4426T>C
|
NP_000486.1:p.Cys1476Arg
|
|
NM_033380.3:c.4444T>C
MANE Select
|
NP_203699.1:p.Cys1482Arg
|
|