ENST00000673913.2:c.1681+129G>T
|
ENSP00000501161.2:n.1681+129G>T
|
|
ENST00000710286.1:c.2038+129G>T
|
ENSP00000518176.1:n.2038+129G>T
|
|
ENST00000673903.1:c.1306+129G>T
|
ENSP00000501257.1:n.1306+129G>T
|
|
ENST00000673913.1:c.421+129G>T
|
ENSP00000501161.1:n.421+129G>T
|
|
ENST00000302118.5:c.1681+129G>T
MANE Select
|
ENSP00000303208.5:n.1681+129G>T
|
|
ENST00000490692.1:n.2227+1145G>T
|
|
|
NM_174936.3:c.1681+129G>T , LRG_275t1:c.1681+129G>T
|
NP_777596.2:n.1681+129G>T
|
|
NR_110451.1:n.1288+129G>T
|
|
|
XM_011541193.1:c.802+129G>T
|
XP_011539495.1:n.802+129G>T
|
|
NM_174936.4:c.1681+129G>T
MANE Select
|
NP_777596.2:n.1681+129G>T
|
|
NR_110451.2:n.1288+129G>T
|
|
|