|
NM_000073.3:c.484-1G>A
MANE Select
|
NP_000064.1:n.484-1G>A
|
|
ENST00000532917.3:c.484-1G>A
MANE Select
|
ENSP00000431445.2:n.484-1G>A
|
|
NM_000073.2:c.484-1G>A , LRG_39t1:c.484-1G>A
|
NP_000064.1:n.484-1G>A
|
|
ENST00000292144.8:c.*541-1G>A
|
ENSP00000292144.4:n.*541-1G>A
|
|
ENST00000392883.6:c.172-1G>A
|
ENSP00000376621.2:n.172-1G>A
|
|
ENST00000532903.1:n.560-1G>A
|
|
|
ENST00000532917.1:c.484-1G>A
|
ENSP00000431445.1:n.484-1G>A
|
|
XM_006718941.2:c.484-1G>A
|
XP_006719004.1:n.484-1G>A
|
|
XM_006718941.3:c.484-1G>A
|
XP_006719004.1:n.484-1G>A
|