ENST00000394867.9:n.1531+238G>A
|
|
|
ENST00000688002.1:n.3243+238G>A
|
|
|
ENST00000688751.1:n.228+238G>A
|
|
|
ENST00000689792.1:n.996+238G>A
|
|
|
ENST00000262948.10:c.1092+238G>A
MANE Select
|
ENSP00000262948.4:n.1092+238G>A
|
|
ENST00000262948.9:c.1092+238G>A
|
ENSP00000262948.3:n.1092+238G>A
|
|
ENST00000394867.8:c.801+238G>A
|
ENSP00000378336.1:n.801+238G>A
|
|
ENST00000597263.5:n.277+238G>A
|
|
|
ENST00000599021.1:c.202+238G>A
|
|
|
ENST00000600584.5:n.2541+238G>A
|
|
|
ENST00000601786.5:n.1393+238G>A
|
|
|
NM_030662.3:c.1092+238G>A , LRG_750t1:c.1092+238G>A
|
NP_109587.1:n.1092+238G>A
|
|
XM_006722799.2:c.813+238G>A
|
XP_006722862.1:n.813+238G>A
|
|
XM_011528133.1:c.522+238G>A
|
XP_011526435.1:n.522+238G>A
|
|
NM_030662.4:c.1092+238G>A
MANE Select
|
NP_109587.1:n.1092+238G>A
|
|