ENST00000553443.6:c.939+19662C>T
MANE Select
|
ENSP00000451131.1:n.939+19662C>T
|
|
ENST00000533625.5:c.939+19662C>T
|
ENSP00000451566.1:n.939+19662C>T
|
|
ENST00000553443.5:c.939+19662C>T
|
ENSP00000451131.1:n.939+19662C>T
|
|
NM_001310135.1:c.987+19662C>T
|
NP_001297064.1:n.987+19662C>T
|
|
XM_011537432.1:c.987+19662C>T
|
XP_011535734.1:n.987+19662C>T
|
|
XR_943762.1:n.1844+19662C>T
|
|
|
XM_011537432.2:c.987+19662C>T
|
XP_011535734.1:n.987+19662C>T
|
|
XM_017021254.1:c.987+19662C>T
|
XP_016876743.1:n.987+19662C>T
|
|
XM_017021255.1:c.987+19662C>T
|
XP_016876744.1:n.987+19662C>T
|
|
XM_017021257.1:c.987+19662C>T
|
XP_016876746.1:n.987+19662C>T
|
|
XM_024449560.1:c.987+19662C>T
|
XP_024305328.1:n.987+19662C>T
|
|
XR_001750287.1:n.1844+19662C>T
|
|
|
XR_943762.2:n.1844+19662C>T
|
|
|
NM_001310135.2:c.987+19662C>T
|
NP_001297064.1:n.987+19662C>T
|
|
NM_001310135.3:c.987+19662C>T
|
NP_001297064.1:n.987+19662C>T
|
|
NM_001310135.5:c.939+19662C>T
MANE Select
|
NP_001297064.2:n.939+19662C>T
|
|