ENST00000270570.8:c.922-138G>T
MANE Select
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ENSP00000270570.4:n.922-138G>T
|
|
ENST00000395585.5:c.922-138G>T
|
ENSP00000378951.1:n.922-138G>T
|
|
ENST00000436810.6:c.853-138G>T
|
ENSP00000407155.2:n.853-138G>T
|
|
ENST00000495425.6:n.365-138G>T
|
|
|
ENST00000497548.5:n.1068+3988G>T
|
|
|
ENST00000571335.5:c.337-138G>T
|
ENSP00000462630.1:n.337-138G>T
|
|
ENST00000573009.1:n.232-120G>T
|
|
|
ENST00000575023.5:c.498+10373G>T
|
ENSP00000460164.1:n.498+10373G>T
|
|
ENST00000575377.5:n.187-138G>T
|
|
|
NM_018242.2:c.922-138G>T
|
NP_060712.2:n.922-138G>T
|
|
NM_018242.3:c.922-138G>T
MANE Select
|
NP_060712.2:n.922-138G>T
|
|