ENST00000553443.6:c.-16+1153C>A
MANE Select
|
ENSP00000451131.1:n.-16+1153C>A
|
|
ENST00000556845.1:c.-155+1153C>A
|
ENSP00000450572.1:n.-155+1153C>A
|
|
NM_001310135.1:c.33+1153C>A
|
NP_001297064.1:n.33+1153C>A
|
|
XM_011537432.1:c.33+1153C>A
|
XP_011535734.1:n.33+1153C>A
|
|
XR_943762.1:n.890+1153C>A
|
|
|
XM_011537432.2:c.33+1153C>A
|
XP_011535734.1:n.33+1153C>A
|
|
XM_017021254.1:c.33+1153C>A
|
XP_016876743.1:n.33+1153C>A
|
|
XM_017021255.1:c.33+1153C>A
|
XP_016876744.1:n.33+1153C>A
|
|
XM_017021257.1:c.33+1153C>A
|
XP_016876746.1:n.33+1153C>A
|
|
XM_024449560.1:c.33+1153C>A
|
XP_024305328.1:n.33+1153C>A
|
|
XR_001750287.1:n.890+1153C>A
|
|
|
XR_943762.2:n.890+1153C>A
|
|
|
NM_001310135.2:c.33+1153C>A
|
NP_001297064.1:n.33+1153C>A
|
|
NM_001310135.3:c.33+1153C>A
|
NP_001297064.1:n.33+1153C>A
|
|
NM_001310135.5:c.-16+1153C>A
MANE Select
|
NP_001297064.2:n.-16+1153C>A
|
|