ENST00000225609.10:c.627C>A
MANE Select
|
ENSP00000225609.5:p.Phe209Leu
|
|
ENST00000225609.9:c.627C>A
|
ENSP00000225609.5:p.Phe209Leu
|
|
ENST00000395844.8:c.595C>A
|
ENSP00000379185.3:p.Arg199Ser
|
|
ENST00000477745.5:n.625C>A
|
|
|
ENST00000488375.2:n.485C>A
|
|
|
ENST00000581006.5:c.426+17897C>A
|
ENSP00000462432.1:n.426+17897C>A
|
|
ENST00000596678.2:c.169C>A
|
ENSP00000470064.2:p.Arg57Ser
|
|
ENST00000613719.1:n.987+187C>A
|
|
|
NM_004278.3:c.627C>A
|
NP_004269.1:p.Phe209Leu
|
|
XR_243571.2:n.1625C>A
|
|
|
XM_017025349.1:c.*791C>A
|
XP_016880838.1:n.*791C>A
|
|
XM_017025350.1:c.*791C>A
|
XP_016880839.1:n.*791C>A
|
|
XM_017025352.1:c.627C>A
|
XP_016880841.1:p.Phe209Leu
|
|
XM_017025353.1:c.627C>A
|
XP_016880842.1:p.Phe209Leu
|
|
XM_017025354.1:c.595C>A
|
XP_016880843.1:p.Arg199Ser
|
|
XM_017025355.1:c.595C>A
|
XP_016880844.1:p.Arg199Ser
|
|
XM_017025356.1:c.*1104C>A
|
XP_016880845.1:n.*1104C>A
|
|
NM_004278.4:c.627C>A
MANE Select
|
NP_004269.1:p.Phe209Leu
|
|