ENST00000477226.6:n.1323G>A
|
|
|
ENST00000683013.1:n.1237G>A
|
|
|
ENST00000373960.4:c.*436G>A
MANE Select
|
ENSP00000363071.3:n.*436G>A
|
|
ENST00000373960.3:c.*436G>A
|
ENSP00000363071.3:n.*436G>A
|
|
NM_001927.3:c.*436G>A , LRG_380t1:c.*436G>A
|
NP_001918.3:n.*436G>A
|
|
NM_001927.4:c.*436G>A
MANE Select
|
NP_001918.3:n.*436G>A
|
|
NM_001382708.1:c.*436G>A
|
NP_001369637.1:n.*436G>A
|
|
NM_001382709.1:c.*436G>A
|
NP_001369638.1:n.*436G>A
|
|
NM_001382710.1:c.*436G>A
|
NP_001369639.1:n.*436G>A
|
|
NM_001382711.1:c.*436G>A
|
NP_001369640.1:n.*436G>A
|
|
NM_001382712.1:c.1372-127G>A
|
NP_001369641.1:n.1372-127G>A
|
|
NM_001382713.1:c.*436G>A
|
NP_001369642.1:n.*436G>A
|
|