|
ENST00000560968.6:c.717G>T
|
ENSP00000453965.2:p.Ala239=
|
|
|
ENST00000257555.11:c.717G>T
MANE Select
|
ENSP00000257555.5:p.Ala239=
|
|
|
ENST00000257555.10:c.717G>T
|
ENSP00000257555.4:p.Ala239=
|
|
|
ENST00000400024.6:c.717G>T
|
ENSP00000476181.1:p.Ala239=
|
|
|
ENST00000402929.5:n.852G>T
|
|
|
|
ENST00000535955.5:n.43-3324G>T
|
|
|
|
ENST00000538626.2:n.191-3324G>T
|
|
|
|
ENST00000538646.5:c.530G>T
|
ENSP00000443964.1:p.Arg177Leu
|
|
|
ENST00000540108.1:c.*157G>T
|
ENSP00000445445.1:n.*157G>T
|
|
|
ENST00000541395.5:c.717G>T
|
ENSP00000443112.1:p.Ala239=
|
|
|
ENST00000541924.5:c.713+461G>T
|
ENSP00000440361.1:n.713+461G>T
|
|
|
ENST00000543427.5:c.633+541G>T
|
ENSP00000439721.2:n.633+541G>T
|
|
|
ENST00000544413.2:c.717G>T
|
ENSP00000438804.1:p.Ala239=
|
|
|
ENST00000544574.5:c.73-2450G>T
|
ENSP00000438565.1:n.73-2450G>T
|
|
|
ENST00000560968.5:c.860G>T
|
|
|
|
ENST00000615446.4:c.-257-2095G>T
|
ENSP00000483994.1:n.-257-2095G>T
|
|
|
ENST00000617366.4:c.586+588G>T
|
ENSP00000481967.1:n.586+588G>T
|
|
|
NM_000545.5:c.717G>T , LRG_522t1:c.717G>T
|
NP_000536.5:p.Ala239=
|
|
|
NM_000545.6:c.717G>T
|
NP_000536.5:p.Ala239=
|
|
|
NM_001306179.1:c.717G>T
|
NP_001293108.1:p.Ala239=
|
|
|
XM_005253931.2:c.717G>T
|
XP_005253988.1:p.Ala239=
|
|
|
XM_024449168.1:c.717G>T
|
XP_024304936.1:p.Ala239=
|
|
|
NM_000545.8:c.717G>T
MANE Select
|
NP_000536.6:p.Ala239=
|
|
|
NM_001306179.2:c.717G>T
|
NP_001293108.2:p.Ala239=
|
|
