ENST00000377453.9:c.*251G>T
(CLN5)
MANE Select
|
ENSP00000366673.5:n.*251G>T
|
|
ENST00000616833.6:c.*770G>T
(CLN5)
|
ENSP00000479547.3:n.*770G>T
|
|
ENST00000635838.1:c.174+5093G>T
|
|
|
ENST00000635905.1:n.566+5093G>T
(CLN5)
|
|
|
ENST00000635915.1:c.1326G>T
(CLN5)
|
|
|
ENST00000636183.2:c.*251G>T
(CLN5)
|
ENSP00000490181.2:n.*251G>T
|
|
ENST00000636525.2:c.565+5093G>T
(CLN5)
|
ENSP00000490078.2:n.565+5093G>T
|
|
ENST00000636681.1:c.*1019G>T
(CLN5)
|
ENSP00000489922.1:n.*1019G>T
|
|
ENST00000636705.1:c.1164G>T
(CLN5)
|
|
|
ENST00000636767.2:c.565+5093G>T
(CLN5)
|
ENSP00000489855.2:n.565+5093G>T
|
|
ENST00000636780.2:c.*777G>T
(CLN5)
|
ENSP00000489809.2:n.*777G>T
|
|
ENST00000637192.1:c.213+5093G>T
|
|
|
ENST00000637278.1:n.1654G>T
(CLN5)
|
|
|
ENST00000637397.2:c.565+5093G>T
(CLN5)
|
ENSP00000490422.2:n.565+5093G>T
|
|
ENST00000638101.1:c.169+5093G>T
|
ENSP00000490535.1:n.169+5093G>T
|
|
ENST00000638147.2:c.565+5093G>T
|
ENSP00000490953.2:n.565+5093G>T
|
|
ENST00000377453.7:c.*251G>T
(CLN5)
|
ENSP00000366673.3:n.*251G>T
|
|
ENST00000477982.2:n.1089C>A
(FBXL3)
|
|
|
ENST00000485797.2:n.174-8269C>A
(FBXL3)
|
|
|
ENST00000616833.4:c.*251G>T
(CLN5)
|
ENSP00000479547.1:n.*251G>T
|
|
NM_006493.2:c.*251G>T , LRG_692t1:c.*251G>T
(CLN5)
|
NP_006484.1:n.*251G>T
|
|
NM_001366624.1:c.*777G>T
(CLN5)
|
NP_001353553.1:n.*777G>T
|
|
NM_006493.3:c.*251G>T
(CLN5)
|
NP_006484.2:n.*251G>T
|
|
XM_017020538.2:c.644-8269C>A
(FBXL3)
|
XP_016876027.1:n.644-8269C>A
|
|
NM_001366624.2:c.*777G>T
(CLN5)
|
NP_001353553.1:n.*777G>T
|
|
NM_006493.4:c.*251G>T
(CLN5)
MANE Select
|
NP_006484.2:n.*251G>T
|
|