|
ENST00000377453.9:c.484G>A
(CLN5)
MANE Select
|
ENSP00000366673.5:p.Gly162Ser
|
|
|
ENST00000485938.4:c.484G>A
(CLN5)
|
ENSP00000482959.3:p.Gly162Ser
|
|
|
ENST00000616833.6:c.484G>A
(CLN5)
|
ENSP00000479547.3:p.Gly162Ser
|
|
|
ENST00000635838.1:c.93G>A
|
|
|
|
ENST00000635905.1:n.485G>A
(CLN5)
|
|
|
|
ENST00000635915.1:c.482G>A
(CLN5)
|
|
|
|
ENST00000635989.1:n.551G>A
(CLN5)
|
|
|
|
ENST00000636183.2:c.484G>A
(CLN5)
|
ENSP00000490181.2:p.Gly162Ser
|
|
|
ENST00000636520.1:n.1996G>A
(CLN5)
|
|
|
|
ENST00000636525.2:c.484G>A
(CLN5)
|
ENSP00000490078.2:p.Gly162Ser
|
|
|
ENST00000636602.1:n.430G>A
(CLN5)
|
|
|
|
ENST00000636681.1:c.*175G>A
(CLN5)
|
ENSP00000489922.1:n.*175G>A
|
|
|
ENST00000636705.1:c.320G>A
(CLN5)
|
|
|
|
ENST00000636767.2:c.484G>A
(CLN5)
|
ENSP00000489855.2:p.Gly162Ser
|
|
|
ENST00000636780.2:c.484G>A
(CLN5)
|
ENSP00000489809.2:p.Gly162Ser
|
|
|
ENST00000637192.1:c.132G>A
|
|
|
|
ENST00000637278.1:n.810G>A
(CLN5)
|
|
|
|
ENST00000637397.2:c.484G>A
(CLN5)
|
ENSP00000490422.2:p.Gly162Ser
|
|
|
ENST00000637537.2:c.484G>A
(CLN5)
|
ENSP00000489711.2:p.Gly162Ser
|
|
|
ENST00000638101.1:c.88G>A
|
ENSP00000490535.1:p.Gly30Ser
|
|
|
ENST00000638147.2:c.484G>A
|
ENSP00000490953.2:p.Gly162Ser
|
|
|
ENST00000377453.7:c.631G>A
(CLN5)
|
ENSP00000366673.3:p.Gly211Ser
|
|
|
ENST00000485797.2:n.174-3095C>T
(FBXL3)
|
|
|
|
ENST00000485938.2:c.467G>A
(CLN5)
|
|
|
|
ENST00000616833.4:c.484G>A
(CLN5)
|
ENSP00000479547.1:p.Gly162Ser
|
|
|
NM_006493.2:c.631G>A , LRG_692t1:c.631G>A
(CLN5)
|
NP_006484.1:p.Gly211Ser
|
|
|
XM_011534917.1:c.631G>A
(CLN5)
|
XP_011533219.1:p.Gly211Ser
|
|
|
NM_001366624.1:c.484G>A
(CLN5)
|
NP_001353553.1:p.Gly162Ser
|
|
|
NM_006493.3:c.484G>A
(CLN5)
|
NP_006484.2:p.Gly162Ser
|
|
|
XM_017020538.2:c.644-3095C>T
(FBXL3)
|
XP_016876027.1:n.644-3095C>T
|
|
|
NM_001366624.2:c.484G>A
(CLN5)
|
NP_001353553.1:p.Gly162Ser
|
|
|
NM_006493.4:c.484G>A
(CLN5)
MANE Select
|
NP_006484.2:p.Gly162Ser
|
|
