ENST00000560968.6:c.*248+3G>A
|
ENSP00000453965.2:n.*248+3G>A
|
|
ENST00000257555.11:c.1501+3G>A
MANE Select
|
ENSP00000257555.5:n.1501+3G>A
|
|
ENST00000257555.10:c.1501+3G>A
|
ENSP00000257555.4:n.1501+3G>A
|
|
ENST00000400024.6:c.1504G>A
|
ENSP00000476181.1:p.Glu502Lys
|
|
ENST00000402929.5:n.2370G>A
|
|
|
ENST00000535955.5:n.220G>A
|
|
|
ENST00000538626.2:n.368G>A
|
|
|
ENST00000538646.5:c.*480G>A
|
ENSP00000443964.1:n.*480G>A
|
|
ENST00000540108.1:c.*941+3G>A
|
ENSP00000445445.1:n.*941+3G>A
|
|
ENST00000541395.5:c.1501+3G>A
|
ENSP00000443112.1:n.1501+3G>A
|
|
ENST00000541924.5:c.*518G>A
|
ENSP00000440361.1:n.*518G>A
|
|
ENST00000543255.1:n.548G>A
|
|
|
ENST00000543427.5:c.964+3G>A
|
ENSP00000439721.2:n.964+3G>A
|
|
ENST00000544413.2:c.1501+3G>A
|
ENSP00000438804.1:n.1501+3G>A
|
|
ENST00000544574.5:c.*267G>A
|
ENSP00000438565.1:n.*267G>A
|
|
ENST00000560968.5:c.1318+3G>A
|
|
|
ENST00000615446.4:c.289+3G>A
|
ENSP00000483994.1:n.289+3G>A
|
|
ENST00000617366.4:c.618+3G>A
|
ENSP00000481967.1:n.618+3G>A
|
|
NM_000545.5:c.1501+3G>A , LRG_522t1:c.1501+3G>A
|
NP_000536.5:n.1501+3G>A
|
|
NM_000545.6:c.1501+3G>A
|
NP_000536.5:n.1501+3G>A
|
|
NM_001306179.1:c.1501+3G>A
|
NP_001293108.1:n.1501+3G>A
|
|
XM_005253931.2:c.1501+3G>A
|
XP_005253988.1:n.1501+3G>A
|
|
XM_024449168.1:c.1501+3G>A
|
XP_024304936.1:n.1501+3G>A
|
|
NM_000545.8:c.1501+3G>A
MANE Select
|
NP_000536.6:n.1501+3G>A
|
|
NM_001306179.2:c.1501+3G>A
|
NP_001293108.2:n.1501+3G>A
|
|