|
ENST00000377453.9:c.793G>T
(CLN5)
MANE Select
|
ENSP00000366673.5:p.Glu265Ter
|
|
|
ENST00000616833.6:c.*235G>T
(CLN5)
|
ENSP00000479547.3:n.*235G>T
|
|
|
ENST00000635838.1:c.174+4558G>T
|
|
|
|
ENST00000635905.1:n.566+4558G>T
(CLN5)
|
|
|
|
ENST00000635915.1:c.791G>T
(CLN5)
|
|
|
|
ENST00000636183.2:c.793G>T
(CLN5)
|
ENSP00000490181.2:p.Glu265Ter
|
|
|
ENST00000636525.2:c.565+4558G>T
(CLN5)
|
ENSP00000490078.2:n.565+4558G>T
|
|
|
ENST00000636681.1:c.*484G>T
(CLN5)
|
ENSP00000489922.1:n.*484G>T
|
|
|
ENST00000636705.1:c.629G>T
(CLN5)
|
|
|
|
ENST00000636767.2:c.565+4558G>T
(CLN5)
|
ENSP00000489855.2:n.565+4558G>T
|
|
|
ENST00000636780.2:c.*242G>T
(CLN5)
|
ENSP00000489809.2:n.*242G>T
|
|
|
ENST00000637192.1:c.213+4558G>T
|
|
|
|
ENST00000637278.1:n.1119G>T
(CLN5)
|
|
|
|
ENST00000637397.2:c.565+4558G>T
(CLN5)
|
ENSP00000490422.2:n.565+4558G>T
|
|
|
ENST00000638101.1:c.169+4558G>T
|
ENSP00000490535.1:n.169+4558G>T
|
|
|
ENST00000638147.2:c.565+4558G>T
|
ENSP00000490953.2:n.565+4558G>T
|
|
|
ENST00000377453.7:c.940G>T
(CLN5)
|
ENSP00000366673.3:p.Glu314Ter
|
|
|
ENST00000477982.2:n.1624C>A
(FBXL3)
|
|
|
|
ENST00000485797.2:n.174-7734C>A
(FBXL3)
|
|
|
|
ENST00000616833.4:c.793G>T
(CLN5)
|
ENSP00000479547.1:p.Glu265Ter
|
|
|
NM_006493.2:c.940G>T , LRG_692t1:c.940G>T
(CLN5)
|
NP_006484.1:p.Glu314Ter
|
|
|
XM_011534917.1:c.*242G>T
(CLN5)
|
XP_011533219.1:n.*242G>T
|
|
|
NM_001366624.1:c.*242G>T
(CLN5)
|
NP_001353553.1:n.*242G>T
|
|
|
NM_006493.3:c.793G>T
(CLN5)
|
NP_006484.2:p.Glu265Ter
|
|
|
XM_017020538.2:c.644-7734C>A
(FBXL3)
|
XP_016876027.1:n.644-7734C>A
|
|
|
NM_001366624.2:c.*242G>T
(CLN5)
|
NP_001353553.1:n.*242G>T
|
|
|
NM_006493.4:c.793G>T
(CLN5)
MANE Select
|
NP_006484.2:p.Glu265Ter
|
|
