ENST00000394867.9:n.1532-141C>T
|
|
|
ENST00000688002.1:n.3244-141C>T
|
|
|
ENST00000688751.1:n.229-141C>T
|
|
|
ENST00000689792.1:n.997-141C>T
|
|
|
ENST00000262948.10:c.1093-141C>T
MANE Select
|
ENSP00000262948.4:n.1093-141C>T
|
|
ENST00000262948.9:c.1093-141C>T
|
ENSP00000262948.3:n.1093-141C>T
|
|
ENST00000394867.8:c.802-141C>T
|
ENSP00000378336.1:n.802-141C>T
|
|
ENST00000597263.5:n.278-141C>T
|
|
|
ENST00000599021.1:c.203-141C>T
|
|
|
ENST00000600584.5:n.2542-141C>T
|
|
|
ENST00000601786.5:n.1394-141C>T
|
|
|
NM_030662.3:c.1093-141C>T , LRG_750t1:c.1093-141C>T
|
NP_109587.1:n.1093-141C>T
|
|
XM_006722799.2:c.814-141C>T
|
XP_006722862.1:n.814-141C>T
|
|
XM_011528133.1:c.523-141C>T
|
XP_011526435.1:n.523-141C>T
|
|
NM_030662.4:c.1093-141C>T
MANE Select
|
NP_109587.1:n.1093-141C>T
|
|