|
NM_005147.6:c.1264A>C
MANE Select
|
NP_005138.3:p.Ser422Arg
|
|
ENST00000262375.11:c.1264A>C
MANE Select
|
ENSP00000262375.4:p.Ser422Arg
|
|
NM_001135110.2:c.1264A>C
|
NP_001128582.1:p.Ser422Arg
|
|
NM_001135110.3:c.1264A>C
|
NP_001128582.1:p.Ser422Arg
|
|
NM_001286516.1:c.805A>C
|
NP_001273445.1:p.Ser269Arg
|
|
NM_001286516.2:c.805A>C
|
NP_001273445.1:p.Ser269Arg
|
|
NM_005147.5:c.1264A>C
|
NP_005138.3:p.Ser422Arg
|
|
ENST00000262375.10:c.1264A>C
|
ENSP00000262375.4:p.Ser422Arg
|
|
ENST00000355296.8:c.1264A>C
|
ENSP00000347445.4:p.Ser422Arg
|
|
ENST00000431375.6:c.805A>C
|
ENSP00000393970.2:p.Ser269Arg
|
|
ENST00000576180.1:n.869A>C
|
|
|
ENST00000576911.5:c.*618A>C
|
ENSP00000459098.1:n.*618A>C
|