ENST00000246337.9:c.996C>T
MANE Select
|
ENSP00000246337.4:p.Arg332=
|
|
ENST00000491773.6:c.753C>T
|
ENSP00000498551.1:p.Arg251=
|
|
ENST00000636293.1:c.858C>T
|
ENSP00000490710.1:p.Arg286=
|
|
ENST00000636836.1:c.*32C>T
|
ENSP00000490594.1:n.*32C>T
|
|
ENST00000651476.1:c.891C>T
|
ENSP00000498668.1:p.Arg297=
|
|
ENST00000652165.1:c.753C>T
|
ENSP00000498295.1:p.Arg251=
|
|
ENST00000652287.1:c.933C>T
|
ENSP00000498413.1:p.Arg311=
|
|
ENST00000652514.1:c.957C>T
|
ENSP00000498635.1:n.957C>T
|
|
ENST00000246337.8:c.996C>T
|
ENSP00000246337.4:p.Arg332=
|
|
ENST00000465678.1:n.741C>T
|
|
|
ENST00000466193.1:n.522C>T
|
|
|
ENST00000472254.1:n.749C>T
|
|
|
ENST00000494399.5:n.1663C>T
|
|
|
NM_000374.4:c.996C>T
|
NP_000365.3:p.Arg332=
|
|
NR_036510.1:n.1179C>T
|
|
|
XM_005271169.1:c.780C>T
|
XP_005271226.1:p.Arg260=
|
|
XM_005271170.1:c.780C>T
|
XP_005271227.1:p.Arg260=
|
|
XM_011542080.1:c.933C>T
|
XP_011540382.1:p.Arg311=
|
|
XM_011542081.1:c.828C>T
|
XP_011540383.1:p.Arg276=
|
|
NM_000374.5:c.996C>T
MANE Select
|
NP_000365.3:p.Arg332=
|
|
NR_158184.1:n.1077C>T
|
|
|
NR_158185.1:n.1027C>T
|
|
|
NR_036510.2:n.1058C>T
|
|
|