ENST00000369538.4:c.1336T>C
|
ENSP00000358551.4:p.Cys446Arg
|
|
ENST00000520113.7:c.1348T>C
MANE Select
|
ENSP00000430075.3:p.Cys450Arg
|
|
ENST00000637080.1:c.1131T>C
|
ENSP00000489753.1:n.1131T>C
|
|
ENST00000639077.1:n.1013T>C
|
|
|
ENST00000369538.3:c.1435T>C
|
ENSP00000358551.3:p.Cys479Arg
|
|
ENST00000520113.6:c.1447T>C
|
ENSP00000430075.2:p.Cys483Arg
|
|
NM_000036.2:c.1447T>C
|
NP_000027.2:p.Cys483Arg
|
|
NM_001172626.1:c.1435T>C
|
NP_001166097.1:p.Cys479Arg
|
|
NM_000036.3:c.1348T>C
MANE Select
|
NP_000027.3:p.Cys450Arg
|
|
NM_001172626.2:c.1336T>C
|
NP_001166097.2:p.Cys446Arg
|
|