|
NM_021939.4:c.*760G>A
MANE Select
|
NP_068758.3:n.*760G>A
|
|
ENST00000321562.9:c.*760G>A
MANE Select
|
ENSP00000317232.4:n.*760G>A
|
|
NM_021939.3:c.*760G>A , LRG_12t1:c.*760G>A
|
NP_068758.3:n.*760G>A
|
|
ENST00000321562.8:c.*760G>A
|
ENSP00000317232.4:n.*760G>A
|
|
ENST00000455106.1:c.1920G>A
|
|
|
ENST00000489591.5:c.*2293G>A
|
ENSP00000466352.1:n.*2293G>A
|
|
XM_011525099.1:c.*760G>A
|
XP_011523401.1:n.*760G>A
|
|
XM_011525099.3:c.*760G>A
|
XP_011523401.1:n.*760G>A
|
|
XM_011525100.1:c.*760G>A
|
XP_011523402.1:n.*760G>A
|
|
XM_011525100.2:c.*760G>A
|
XP_011523402.1:n.*760G>A
|