ENST00000270570.8:c.922-158G>T
MANE Select
|
ENSP00000270570.4:n.922-158G>T
|
|
ENST00000395585.5:c.922-158G>T
|
ENSP00000378951.1:n.922-158G>T
|
|
ENST00000436810.6:c.853-158G>T
|
ENSP00000407155.2:n.853-158G>T
|
|
ENST00000495425.6:n.365-158G>T
|
|
|
ENST00000497548.5:n.1068+3968G>T
|
|
|
ENST00000571335.5:c.337-158G>T
|
ENSP00000462630.1:n.337-158G>T
|
|
ENST00000573009.1:n.232-140G>T
|
|
|
ENST00000575023.5:c.498+10353G>T
|
ENSP00000460164.1:n.498+10353G>T
|
|
ENST00000575377.5:n.187-158G>T
|
|
|
NM_018242.2:c.922-158G>T
|
NP_060712.2:n.922-158G>T
|
|
NM_018242.3:c.922-158G>T
MANE Select
|
NP_060712.2:n.922-158G>T
|
|