ENST00000697337.1:c.*2558T>A
|
ENSP00000513259.1:n.*2558T>A
|
|
ENST00000697338.1:c.1670T>A
|
ENSP00000513260.1:n.1670T>A
|
|
ENST00000697339.1:c.856T>A
|
ENSP00000513261.1:p.Ser286Thr
|
|
ENST00000697340.1:c.*539T>A
|
ENSP00000513262.1:n.*539T>A
|
|
ENST00000697341.1:n.1792T>A
|
|
|
ENST00000313735.11:c.1822T>A
MANE Select
|
ENSP00000327251.6:p.Ser608Thr
|
|
ENST00000646938.1:c.1819T>A
|
ENSP00000494870.1:p.Ser607Thr
|
|
ENST00000313735.10:c.1822T>A
|
ENSP00000327251.6:p.Ser608Thr
|
|
ENST00000621962.1:c.1705T>A
|
ENSP00000482291.1:p.Ser569Thr
|
|
NM_000625.4:c.1822T>A
MANE Select
|
NP_000616.3:p.Ser608Thr
|
|
XM_011524859.1:c.1822T>A
|
XP_011523161.1:p.Ser608Thr
|
|
XM_011524860.1:c.1819T>A
|
XP_011523162.1:p.Ser607Thr
|
|
XM_011524861.1:c.1822T>A
|
XP_011523163.1:p.Ser608Thr
|
|
XM_011524862.1:c.1156T>A
|
XP_011523164.1:p.Ser386Thr
|
|