ENST00000355112.8:c.3652T>C
MANE Select
|
ENSP00000347232.3:p.Cys1218Arg
|
|
ENST00000560559.2:n.2225T>C
|
|
|
ENST00000648453.1:c.3652T>C
|
ENSP00000497646.1:p.Cys1218Arg
|
|
ENST00000680772.1:c.3652T>C
|
ENSP00000506117.1:p.Cys1218Arg
|
|
ENST00000681142.1:c.3652T>C
|
ENSP00000506682.1:p.Cys1218Arg
|
|
ENST00000355112.7:c.3652T>C
|
ENSP00000347232.3:p.Cys1218Arg
|
|
ENST00000558825.5:n.999T>C
|
|
|
ENST00000559724.5:c.*2576T>C
|
ENSP00000453359.1:n.*2576T>C
|
|
ENST00000560136.5:n.1678T>C
|
|
|
ENST00000560509.5:c.3359-4877T>C
|
ENSP00000454158.1:n.3359-4877T>C
|
|
NM_000057.3:c.3652T>C
|
NP_000048.1:p.Cys1218Arg
|
|
NM_001287246.1:c.3652T>C
|
NP_001274175.1:p.Cys1218Arg
|
|
NM_001287247.1:c.3359-4877T>C
|
NP_001274176.1:n.3359-4877T>C
|
|
NM_001287248.1:c.2527T>C
|
NP_001274177.1:p.Cys843Arg
|
|
XM_006720632.2:c.1690T>C
|
XP_006720695.1:p.Cys564Arg
|
|
XM_011521881.1:c.2338T>C
|
XP_011520183.1:p.Cys780Arg
|
|
XM_011521881.2:c.2338T>C
|
XP_011520183.1:p.Cys780Arg
|
|
NM_000057.4:c.3652T>C
MANE Select
|
NP_000048.1:p.Cys1218Arg
|
|
NM_001287246.2:c.3652T>C
|
NP_001274175.1:p.Cys1218Arg
|
|
NM_001287247.2:c.3359-4877T>C
|
NP_001274176.1:n.3359-4877T>C
|
|
NM_001287248.2:c.2527T>C
|
NP_001274177.1:p.Cys843Arg
|
|