ENST00000326828.6:c.805T>C
MANE Select
|
ENSP00000315602.5:p.Cys269Arg
|
|
ENST00000326828.5:c.805T>C
|
ENSP00000315602.5:p.Cys269Arg
|
|
ENST00000348639.7:c.805T>C
|
ENSP00000267951.4:p.Cys269Arg
|
|
ENST00000558903.1:n.512T>C
|
|
|
ENST00000559658.5:c.805T>C
|
ENSP00000452896.1:p.Cys269Arg
|
|
NM_000743.4:c.805T>C
|
NP_000734.2:p.Cys269Arg
|
|
NM_001166694.1:c.805T>C
|
NP_001160166.1:p.Cys269Arg
|
|
NR_046313.1:n.1306T>C
|
|
|
XM_006720382.1:c.604T>C
|
XP_006720445.1:p.Cys202Arg
|
|
XM_011521173.1:c.724T>C
|
XP_011519475.1:p.Cys242Arg
|
|
XM_006720382.3:c.604T>C
|
XP_006720445.1:p.Cys202Arg
|
|
NM_000743.5:c.805T>C
MANE Select
|
NP_000734.2:p.Cys269Arg
|
|
NM_001166694.2:c.805T>C
|
NP_001160166.1:p.Cys269Arg
|
|
NR_046313.2:n.1007T>C
|
|
|