|
NM_000074.3:c.289-27G>T
MANE Select
|
NP_000065.1:n.289-27G>T
|
|
ENST00000370629.7:c.289-27G>T
MANE Select
|
ENSP00000359663.2:n.289-27G>T
|
|
NM_000074.2:c.289-27G>T , LRG_141t1:c.289-27G>T
|
NP_000065.1:n.289-27G>T
|
|
ENST00000370628.2:c.289-27G>T
|
ENSP00000359662.2:n.289-27G>T
|
|
ENST00000370629.6:c.289-27G>T
|
ENSP00000359663.2:n.289-27G>T
|
|
ENST00000695724.1:c.289-2010G>T
|
ENSP00000512122.1:n.289-2010G>T
|
|
ENST00000695725.1:c.157-4693G>T
|
ENSP00000512123.1:n.157-4693G>T
|
|
ENST00000695726.1:n.332-27G>T
|
|
|
ENST00000695729.1:n.1140G>T
|
|