ENST00000477226.6:n.498-98G>T
|
|
|
ENST00000683013.1:n.412-98G>T
|
|
|
ENST00000373960.4:c.1024-98G>T
MANE Select
|
ENSP00000363071.3:n.1024-98G>T
|
|
ENST00000373960.3:c.1024-98G>T
|
ENSP00000363071.3:n.1024-98G>T
|
|
ENST00000477226.5:n.496-98G>T
|
|
|
ENST00000492726.1:n.419-98G>T
|
|
|
NM_001927.3:c.1024-98G>T , LRG_380t1:c.1024-98G>T
|
NP_001918.3:n.1024-98G>T
|
|
NM_001927.4:c.1024-98G>T
MANE Select
|
NP_001918.3:n.1024-98G>T
|
|
NM_001382708.1:c.1021-98G>T
|
NP_001369637.1:n.1021-98G>T
|
|
NM_001382709.1:c.736-242G>T
|
NP_001369638.1:n.736-242G>T
|
|
NM_001382710.1:c.1024-167G>T
|
NP_001369639.1:n.1024-167G>T
|
|
NM_001382711.1:c.1024-119G>T
|
NP_001369640.1:n.1024-119G>T
|
|
NM_001382712.1:c.1024-98G>T
|
NP_001369641.1:n.1024-98G>T
|
|
NM_001382713.1:c.754-98G>T
|
NP_001369642.1:n.754-98G>T
|
|