ENST00000699947.1:c.2134C>T
|
ENSP00000514703.1:p.Arg712Ter
|
|
ENST00000699948.1:c.*447C>T
|
ENSP00000514704.1:n.*447C>T
|
|
ENST00000382745.9:c.2134C>T
MANE Select
|
ENSP00000372193.4:p.Arg712Ter
|
|
ENST00000262318.12:c.2062C>T
|
ENSP00000262318.8:p.Arg688Ter
|
|
ENST00000382745.8:c.2134C>T
|
ENSP00000372193.4:p.Arg712Ter
|
|
ENST00000448525.5:c.2062C>T
|
ENSP00000410907.1:p.Arg688Ter
|
|
ENST00000563642.6:n.2203C>T
|
|
|
ENST00000565092.6:n.1169C>T
|
|
|
ENST00000567836.2:n.375C>T
|
|
|
NM_001114331.2:c.2062C>T
|
NP_001107803.1:p.Arg688Ter
|
|
NM_001287.5:c.2134C>T
|
NP_001278.1:p.Arg712Ter
|
|
XM_011522354.1:c.1960C>T
|
XP_011520656.1:p.Arg654Ter
|
|
NM_001287.6:c.2134C>T
MANE Select
|
NP_001278.1:p.Arg712Ter
|
|
NM_001114331.3:c.2062C>T
|
NP_001107803.1:p.Arg688Ter
|
|