ENST00000649276.2:c.1482G>A
MANE Select
|
ENSP00000497003.1:p.Ala494=
|
|
ENST00000329705.11:c.1009+832G>A
|
ENSP00000331176.7:n.1009+832G>A
|
|
ENST00000332710.8:c.1455G>A
|
ENSP00000331791.4:p.Ala485=
|
|
ENST00000359500.7:c.1009+832G>A
|
ENSP00000352483.3:n.1009+832G>A
|
|
ENST00000621939.1:c.1009+832G>A
|
ENSP00000477982.1:n.1009+832G>A
|
|
NM_005992.1:c.1009+832G>A
|
NP_005983.1:n.1009+832G>A
|
|
NM_080646.1:c.1009+832G>A
|
NP_542377.1:n.1009+832G>A
|
|
NM_080647.1:c.1455G>A , LRG_226t1:c.1455G>A
|
NP_542378.1:p.Ala485=
|
|
XM_006724312.1:c.1455G>A
|
XP_006724375.1:p.Ala485=
|
|
XM_011530351.1:c.1482G>A
|
XP_011528653.1:p.Ala494=
|
|
XM_006724312.2:c.1455G>A
|
XP_006724375.1:p.Ala485=
|
|
XM_017028925.1:c.1605G>A
|
XP_016884414.1:p.Ala535=
|
|
XM_017028926.1:c.1455G>A
|
XP_016884415.1:p.Ala485=
|
|
XM_017028927.1:c.810G>A
|
XP_016884416.1:p.Ala270=
|
|
XM_017028928.1:c.1159+832G>A
|
XP_016884417.1:n.1159+832G>A
|
|
NM_001379200.1:c.1482G>A
MANE Select
|
NP_001366129.1:p.Ala494=
|
|
NM_080646.2:c.1009+832G>A
|
NP_542377.1:n.1009+832G>A
|
|