ENST00000697337.1:c.*2560G>T
|
ENSP00000513259.1:n.*2560G>T
|
|
ENST00000697338.1:c.1672G>T
|
ENSP00000513260.1:n.1672G>T
|
|
ENST00000697339.1:c.858G>T
|
ENSP00000513261.1:p.Ser286=
|
|
ENST00000697340.1:c.*541G>T
|
ENSP00000513262.1:n.*541G>T
|
|
ENST00000697341.1:n.1794G>T
|
|
|
ENST00000313735.11:c.1824G>T
MANE Select
|
ENSP00000327251.6:p.Ser608=
|
|
ENST00000646938.1:c.1821G>T
|
ENSP00000494870.1:p.Ser607=
|
|
ENST00000313735.10:c.1824G>T
|
ENSP00000327251.6:p.Ser608=
|
|
ENST00000621962.1:c.1707G>T
|
ENSP00000482291.1:p.Ser569=
|
|
NM_000625.4:c.1824G>T
MANE Select
|
NP_000616.3:p.Ser608=
|
|
XM_011524859.1:c.1824G>T
|
XP_011523161.1:p.Ser608=
|
|
XM_011524860.1:c.1821G>T
|
XP_011523162.1:p.Ser607=
|
|
XM_011524861.1:c.1824G>T
|
XP_011523163.1:p.Ser608=
|
|
XM_011524862.1:c.1158G>T
|
XP_011523164.1:p.Ser386=
|
|