|
ENST00000560968.6:c.*166G>C
|
ENSP00000453965.2:n.*166G>C
|
|
|
ENST00000257555.11:c.1419G>C
MANE Select
|
ENSP00000257555.5:p.Gln473His
|
|
|
ENST00000257555.10:c.1419G>C
|
ENSP00000257555.4:p.Gln473His
|
|
|
ENST00000400024.6:c.1419G>C
|
ENSP00000476181.1:p.Gln473His
|
|
|
ENST00000402929.5:n.2285G>C
|
|
|
|
ENST00000535955.5:n.135G>C
|
|
|
|
ENST00000538626.2:n.283G>C
|
|
|
|
ENST00000538646.5:c.*395G>C
|
ENSP00000443964.1:n.*395G>C
|
|
|
ENST00000540108.1:c.*859G>C
|
ENSP00000445445.1:n.*859G>C
|
|
|
ENST00000541395.5:c.1419G>C
|
ENSP00000443112.1:p.Gln473His
|
|
|
ENST00000541924.5:c.*433G>C
|
ENSP00000440361.1:n.*433G>C
|
|
|
ENST00000543255.1:n.463G>C
|
|
|
|
ENST00000543427.5:c.882G>C
|
ENSP00000439721.2:p.Gln294His
|
|
|
ENST00000544413.2:c.1419G>C
|
ENSP00000438804.1:p.Gln473His
|
|
|
ENST00000544574.5:c.*182G>C
|
ENSP00000438565.1:n.*182G>C
|
|
|
ENST00000560968.5:c.1236G>C
|
|
|
|
ENST00000615446.4:c.207G>C
|
ENSP00000483994.1:p.Gln69His
|
|
|
ENST00000617366.4:c.587-51G>C
|
ENSP00000481967.1:n.587-51G>C
|
|
|
NM_000545.5:c.1419G>C , LRG_522t1:c.1419G>C
|
NP_000536.5:p.Gln473His
|
|
|
NM_000545.6:c.1419G>C
|
NP_000536.5:p.Gln473His
|
|
|
NM_001306179.1:c.1419G>C
|
NP_001293108.1:p.Gln473His
|
|
|
XM_005253931.2:c.1419G>C
|
XP_005253988.1:p.Gln473His
|
|
|
XM_024449168.1:c.1419G>C
|
XP_024304936.1:p.Gln473His
|
|
|
NM_000545.8:c.1419G>C
MANE Select
|
NP_000536.6:p.Gln473His
|
|
|
NM_001306179.2:c.1419G>C
|
NP_001293108.2:p.Gln473His
|
|
