ENST00000477226.6:n.498-160A>G
|
|
|
ENST00000683013.1:n.412-160A>G
|
|
|
ENST00000373960.4:c.1024-160A>G
MANE Select
|
ENSP00000363071.3:n.1024-160A>G
|
|
ENST00000373960.3:c.1024-160A>G
|
ENSP00000363071.3:n.1024-160A>G
|
|
ENST00000477226.5:n.496-160A>G
|
|
|
ENST00000492726.1:n.419-160A>G
|
|
|
NM_001927.3:c.1024-160A>G , LRG_380t1:c.1024-160A>G
|
NP_001918.3:n.1024-160A>G
|
|
NM_001927.4:c.1024-160A>G
MANE Select
|
NP_001918.3:n.1024-160A>G
|
|
NM_001382708.1:c.1021-160A>G
|
NP_001369637.1:n.1021-160A>G
|
|
NM_001382709.1:c.736-304A>G
|
NP_001369638.1:n.736-304A>G
|
|
NM_001382710.1:c.1023+227A>G
|
NP_001369639.1:n.1023+227A>G
|
|
NM_001382711.1:c.1024-181A>G
|
NP_001369640.1:n.1024-181A>G
|
|
NM_001382712.1:c.1024-160A>G
|
NP_001369641.1:n.1024-160A>G
|
|
NM_001382713.1:c.754-160A>G
|
NP_001369642.1:n.754-160A>G
|
|