ENST00000344887.10:c.373-139G>C
MANE Select
|
ENSP00000341838.5:n.373-139G>C
|
|
ENST00000665070.1:c.406-139G>C
|
ENSP00000499482.1:n.406-139G>C
|
|
ENST00000344887.9:c.373-139G>C
|
ENSP00000341838.5:n.373-139G>C
|
|
ENST00000585806.5:n.372-139G>C
|
|
|
ENST00000586669.5:n.381-139G>C
|
|
|
ENST00000587176.5:n.952G>C
|
|
|
ENST00000588882.1:c.298-139G>C
|
ENSP00000466729.1:n.298-139G>C
|
|
ENST00000589864.1:n.62G>C
|
|
|
NM_000363.4:c.373-139G>C , LRG_432t1:c.373-139G>C
|
NP_000354.4:n.373-139G>C
|
|
NM_000363.5:c.373-139G>C
MANE Select
|
NP_000354.4:n.373-139G>C
|
|