|
ENST00000560968.6:c.*208C>T
|
ENSP00000453965.2:n.*208C>T
|
|
|
ENST00000257555.11:c.1461C>T
MANE Select
|
ENSP00000257555.5:p.Ser487=
|
|
|
ENST00000257555.10:c.1461C>T
|
ENSP00000257555.4:p.Ser487=
|
|
|
ENST00000400024.6:c.1461C>T
|
ENSP00000476181.1:p.Ser487=
|
|
|
ENST00000402929.5:n.2327C>T
|
|
|
|
ENST00000535955.5:n.177C>T
|
|
|
|
ENST00000538626.2:n.325C>T
|
|
|
|
ENST00000538646.5:c.*437C>T
|
ENSP00000443964.1:n.*437C>T
|
|
|
ENST00000540108.1:c.*901C>T
|
ENSP00000445445.1:n.*901C>T
|
|
|
ENST00000541395.5:c.1461C>T
|
ENSP00000443112.1:p.Ser487=
|
|
|
ENST00000541924.5:c.*475C>T
|
ENSP00000440361.1:n.*475C>T
|
|
|
ENST00000543255.1:n.505C>T
|
|
|
|
ENST00000543427.5:c.924C>T
|
ENSP00000439721.2:p.Ser308=
|
|
|
ENST00000544413.2:c.1461C>T
|
ENSP00000438804.1:p.Ser487=
|
|
|
ENST00000544574.5:c.*224C>T
|
ENSP00000438565.1:n.*224C>T
|
|
|
ENST00000560968.5:c.1278C>T
|
|
|
|
ENST00000615446.4:c.249C>T
|
ENSP00000483994.1:p.Ser83=
|
|
|
ENST00000617366.4:c.587-9C>T
|
ENSP00000481967.1:n.587-9C>T
|
|
|
NM_000545.5:c.1461C>T , LRG_522t1:c.1461C>T
|
NP_000536.5:p.Ser487=
|
|
|
NM_000545.6:c.1461C>T
|
NP_000536.5:p.Ser487=
|
|
|
NM_001306179.1:c.1461C>T
|
NP_001293108.1:p.Ser487=
|
|
|
XM_005253931.2:c.1461C>T
|
XP_005253988.1:p.Ser487=
|
|
|
XM_024449168.1:c.1461C>T
|
XP_024304936.1:p.Ser487=
|
|
|
NM_000545.8:c.1461C>T
MANE Select
|
NP_000536.6:p.Ser487=
|
|
|
NM_001306179.2:c.1461C>T
|
NP_001293108.2:p.Ser487=
|
|
