|
NM_018417.6:c.1140-114A>G
MANE Select
|
NP_060887.2:n.1140-114A>G
|
|
ENST00000367851.9:c.1140-114A>G
MANE Select
|
ENSP00000356825.4:n.1140-114A>G
|
|
NM_001167749.2:c.681-114A>G
|
NP_001161221.1:n.681-114A>G
|
|
NM_001167749.3:c.681-114A>G
|
NP_001161221.1:n.681-114A>G
|
|
NM_001297772.1:c.864-114A>G
|
NP_001284701.1:n.864-114A>G
|
|
NM_001297772.2:c.864-114A>G
|
NP_001284701.1:n.864-114A>G
|
|
NM_018417.5:c.1140-114A>G
|
NP_060887.2:n.1140-114A>G
|
|
ENST00000367848.1:c.864-114A>G
|
ENSP00000356822.1:n.864-114A>G
|
|
ENST00000367851.8:c.1140-114A>G
|
ENSP00000356825.4:n.1140-114A>G
|
|
ENST00000545172.5:c.681-114A>G
|
ENSP00000441992.1:n.681-114A>G
|
|
XM_005245330.3:c.1140-114A>G
|
XP_005245387.1:n.1140-114A>G
|
|
XM_005245330.5:c.1140-114A>G
|
XP_005245387.1:n.1140-114A>G
|
|
XM_006711449.2:c.1140-114A>G
|
XP_006711512.1:n.1140-114A>G
|
|
XM_006711449.4:c.1140-114A>G
|
XP_006711512.1:n.1140-114A>G
|
|
XM_011509760.1:c.1140-114A>G
|
XP_011508062.1:n.1140-114A>G
|
|
XM_011509760.3:c.1140-114A>G
|
XP_011508062.1:n.1140-114A>G
|
|
XM_011509761.1:c.1035-114A>G
|
XP_011508063.1:n.1035-114A>G
|
|
XM_011509762.1:c.996-114A>G
|
XP_011508064.1:n.996-114A>G
|
|
XM_011509762.3:c.996-114A>G
|
XP_011508064.1:n.996-114A>G
|
|
XM_011509763.1:c.1140-114A>G
|
XP_011508065.1:n.1140-114A>G
|
|
XM_011509763.3:c.1140-114A>G
|
XP_011508065.1:n.1140-114A>G
|
|
XM_011509764.1:c.891-114A>G
|
XP_011508066.1:n.891-114A>G
|
|
XM_011509765.1:c.864-114A>G
|
XP_011508067.1:n.864-114A>G
|
|
XM_011509766.1:c.1140-114A>G
|
XP_011508068.1:n.1140-114A>G
|
|
XM_011509766.3:c.1140-114A>G
|
XP_011508068.1:n.1140-114A>G
|
|
XM_017001778.2:c.1140-114A>G
|
XP_016857267.1:n.1140-114A>G
|
|
XR_921889.1:n.2749-114A>G
|
|
|
XR_921889.3:n.3612-114A>G
|
|