ENST00000225609.10:c.660+316C>T
MANE Select
|
ENSP00000225609.5:n.660+316C>T
|
|
ENST00000225609.9:c.660+316C>T
|
ENSP00000225609.5:n.660+316C>T
|
|
ENST00000395844.8:c.628+316C>T
|
ENSP00000379185.3:n.628+316C>T
|
|
ENST00000477745.5:n.658+316C>T
|
|
|
ENST00000488375.2:n.518+316C>T
|
|
|
ENST00000581006.5:c.426+18246C>T
|
ENSP00000462432.1:n.426+18246C>T
|
|
ENST00000596678.2:c.202+316C>T
|
ENSP00000470064.2:n.202+316C>T
|
|
ENST00000613719.1:n.987+536C>T
|
|
|
NM_004278.3:c.660+316C>T
|
NP_004269.1:n.660+316C>T
|
|
XR_243571.2:n.1658+316C>T
|
|
|
XM_017025349.1:c.*824+316C>T
|
XP_016880838.1:n.*824+316C>T
|
|
XM_017025350.1:c.*824+316C>T
|
XP_016880839.1:n.*824+316C>T
|
|
XM_017025352.1:c.660+316C>T
|
XP_016880841.1:n.660+316C>T
|
|
XM_017025353.1:c.660+316C>T
|
XP_016880842.1:n.660+316C>T
|
|
XM_017025354.1:c.628+316C>T
|
XP_016880843.1:n.628+316C>T
|
|
XM_017025355.1:c.628+316C>T
|
XP_016880844.1:n.628+316C>T
|
|
XM_017025356.1:c.*1137+316C>T
|
XP_016880845.1:n.*1137+316C>T
|
|
NM_004278.4:c.660+316C>T
MANE Select
|
NP_004269.1:n.660+316C>T
|
|