|
ENST00000560968.6:c.*248+2dup
|
ENSP00000453965.2:n.*248+2dup
|
|
|
ENST00000257555.11:c.1501+2dup
MANE Select
|
ENSP00000257555.5:n.1501+2dup
|
|
|
ENST00000257555.10:c.1501+2dup
|
ENSP00000257555.4:n.1501+2dup
|
|
|
ENST00000400024.6:c.1503dup
|
ENSP00000476181.1:p.Glu502Ter
|
|
|
ENST00000402929.5:n.2369dup
|
|
|
|
ENST00000535955.5:n.219dup
|
|
|
|
ENST00000538626.2:n.367dup
|
|
|
|
ENST00000538646.5:c.*479dup
|
ENSP00000443964.1:n.*479dup
|
|
|
ENST00000540108.1:c.*941+2dup
|
ENSP00000445445.1:n.*941+2dup
|
|
|
ENST00000541395.5:c.1501+2dup
|
ENSP00000443112.1:n.1501+2dup
|
|
|
ENST00000541924.5:c.*517dup
|
ENSP00000440361.1:n.*517dup
|
|
|
ENST00000543255.1:n.547dup
|
|
|
|
ENST00000543427.5:c.964+2dup
|
ENSP00000439721.2:n.964+2dup
|
|
|
ENST00000544413.2:c.1501+2dup
|
ENSP00000438804.1:n.1501+2dup
|
|
|
ENST00000544574.5:c.*266dup
|
ENSP00000438565.1:n.*266dup
|
|
|
ENST00000560968.5:c.1318+2dup
|
|
|
|
ENST00000615446.4:c.289+2dup
|
ENSP00000483994.1:n.289+2dup
|
|
|
ENST00000617366.4:c.618+2dup
|
ENSP00000481967.1:n.618+2dup
|
|
|
NM_000545.5:c.1501+2dup , LRG_522t1:c.1501+2dup
|
NP_000536.5:n.1501+2dup
|
|
|
NM_000545.6:c.1501+2dup
|
NP_000536.5:n.1501+2dup
|
|
|
NM_001306179.1:c.1501+2dup
|
NP_001293108.1:n.1501+2dup
|
|
|
XM_005253931.2:c.1501+2dup
|
XP_005253988.1:n.1501+2dup
|
|
|
XM_024449168.1:c.1501+2dup
|
XP_024304936.1:n.1501+2dup
|
|
|
NM_000545.8:c.1501+2dup
MANE Select
|
NP_000536.6:n.1501+2dup
|
|
|
NM_001306179.2:c.1501+2dup
|
NP_001293108.2:n.1501+2dup
|
|
