ENST00000477226.6:n.498-148C>T
|
|
|
ENST00000683013.1:n.412-148C>T
|
|
|
ENST00000373960.4:c.1024-148C>T
MANE Select
|
ENSP00000363071.3:n.1024-148C>T
|
|
ENST00000373960.3:c.1024-148C>T
|
ENSP00000363071.3:n.1024-148C>T
|
|
ENST00000477226.5:n.496-148C>T
|
|
|
ENST00000492726.1:n.419-148C>T
|
|
|
NM_001927.3:c.1024-148C>T , LRG_380t1:c.1024-148C>T
|
NP_001918.3:n.1024-148C>T
|
|
NM_001927.4:c.1024-148C>T
MANE Select
|
NP_001918.3:n.1024-148C>T
|
|
NM_001382708.1:c.1021-148C>T
|
NP_001369637.1:n.1021-148C>T
|
|
NM_001382709.1:c.736-292C>T
|
NP_001369638.1:n.736-292C>T
|
|
NM_001382710.1:c.1024-217C>T
|
NP_001369639.1:n.1024-217C>T
|
|
NM_001382711.1:c.1024-169C>T
|
NP_001369640.1:n.1024-169C>T
|
|
NM_001382712.1:c.1024-148C>T
|
NP_001369641.1:n.1024-148C>T
|
|
NM_001382713.1:c.754-148C>T
|
NP_001369642.1:n.754-148C>T
|
|