ENST00000225609.10:c.657C>T
MANE Select
|
ENSP00000225609.5:p.Ala219=
|
|
ENST00000225609.9:c.657C>T
|
ENSP00000225609.5:p.Ala219=
|
|
ENST00000395844.8:c.625C>T
|
ENSP00000379185.3:p.Gln209Ter
|
|
ENST00000477745.5:n.655C>T
|
|
|
ENST00000488375.2:n.515C>T
|
|
|
ENST00000581006.5:c.426+17927C>T
|
ENSP00000462432.1:n.426+17927C>T
|
|
ENST00000596678.2:c.199C>T
|
ENSP00000470064.2:p.Gln67Ter
|
|
ENST00000613719.1:n.987+217C>T
|
|
|
NM_004278.3:c.657C>T
|
NP_004269.1:p.Ala219=
|
|
XR_243571.2:n.1655C>T
|
|
|
XM_017025349.1:c.*821C>T
|
XP_016880838.1:n.*821C>T
|
|
XM_017025350.1:c.*821C>T
|
XP_016880839.1:n.*821C>T
|
|
XM_017025352.1:c.657C>T
|
XP_016880841.1:p.Ala219=
|
|
XM_017025353.1:c.657C>T
|
XP_016880842.1:p.Ala219=
|
|
XM_017025354.1:c.625C>T
|
XP_016880843.1:p.Gln209Ter
|
|
XM_017025355.1:c.625C>T
|
XP_016880844.1:p.Gln209Ter
|
|
XM_017025356.1:c.*1134C>T
|
XP_016880845.1:n.*1134C>T
|
|
NM_004278.4:c.657C>T
MANE Select
|
NP_004269.1:p.Ala219=
|
|