ENST00000697337.1:c.*3092+71T>C
|
ENSP00000513259.1:n.*3092+71T>C
|
|
ENST00000697338.1:c.2275T>C
|
ENSP00000513260.1:n.2275T>C
|
|
ENST00000697339.1:c.1390+71T>C
|
ENSP00000513261.1:n.1390+71T>C
|
|
ENST00000697340.1:c.*1144T>C
|
ENSP00000513262.1:n.*1144T>C
|
|
ENST00000697341.1:n.2397T>C
|
|
|
ENST00000313735.11:c.2427T>C
MANE Select
|
ENSP00000327251.6:p.Ser809=
|
|
ENST00000646938.1:c.2424T>C
|
ENSP00000494870.1:p.Ser808=
|
|
ENST00000313735.10:c.2427T>C
|
ENSP00000327251.6:p.Ser809=
|
|
ENST00000621962.1:c.2310T>C
|
ENSP00000482291.1:p.Ser770=
|
|
NM_000625.4:c.2427T>C
MANE Select
|
NP_000616.3:p.Ser809=
|
|
XM_011524859.1:c.2427T>C
|
XP_011523161.1:p.Ser809=
|
|
XM_011524860.1:c.2424T>C
|
XP_011523162.1:p.Ser808=
|
|
XM_011524861.1:c.2356+71T>C
|
XP_011523163.1:n.2356+71T>C
|
|
XM_011524862.1:c.1761T>C
|
XP_011523164.1:p.Ser587=
|
|