ENST00000246337.9:c.1004C>A
MANE Select
|
ENSP00000246337.4:p.Ala335Asp
|
|
ENST00000491773.6:c.761C>A
|
ENSP00000498551.1:p.Ala254Asp
|
|
ENST00000636293.1:c.866C>A
|
ENSP00000490710.1:p.Ala289Asp
|
|
ENST00000636836.1:c.*40C>A
|
ENSP00000490594.1:n.*40C>A
|
|
ENST00000651476.1:c.899C>A
|
ENSP00000498668.1:p.Ala300Asp
|
|
ENST00000652165.1:c.761C>A
|
ENSP00000498295.1:p.Ala254Asp
|
|
ENST00000652287.1:c.941C>A
|
ENSP00000498413.1:p.Ala314Asp
|
|
ENST00000652514.1:c.965C>A
|
ENSP00000498635.1:n.965C>A
|
|
ENST00000246337.8:c.1004C>A
|
ENSP00000246337.4:p.Ala335Asp
|
|
ENST00000465678.1:n.749C>A
|
|
|
ENST00000472254.1:n.757C>A
|
|
|
ENST00000494399.5:n.1671C>A
|
|
|
NM_000374.4:c.1004C>A
|
NP_000365.3:p.Ala335Asp
|
|
NR_036510.1:n.1187C>A
|
|
|
XM_005271169.1:c.788C>A
|
XP_005271226.1:p.Ala263Asp
|
|
XM_005271170.1:c.788C>A
|
XP_005271227.1:p.Ala263Asp
|
|
XM_011542080.1:c.941C>A
|
XP_011540382.1:p.Ala314Asp
|
|
XM_011542081.1:c.836C>A
|
XP_011540383.1:p.Ala279Asp
|
|
NM_000374.5:c.1004C>A
MANE Select
|
NP_000365.3:p.Ala335Asp
|
|
NR_158184.1:n.1085C>A
|
|
|
NR_158185.1:n.1035C>A
|
|
|
NR_036510.2:n.1066C>A
|
|
|