ENST00000225609.10:c.492G>T
MANE Select
|
ENSP00000225609.5:p.Val164=
|
|
ENST00000225609.9:c.492G>T
|
ENSP00000225609.5:p.Val164=
|
|
ENST00000395844.8:c.492G>T
|
ENSP00000379185.3:p.Val164=
|
|
ENST00000477745.5:n.490G>T
|
|
|
ENST00000498772.6:n.509G>T
|
|
|
ENST00000580201.1:n.504G>T
|
|
|
ENST00000581006.5:c.426+13634G>T
|
ENSP00000462432.1:n.426+13634G>T
|
|
ENST00000584797.5:c.492G>T
|
ENSP00000463540.1:p.Val164=
|
|
ENST00000585034.5:c.*86G>T
|
ENSP00000464424.1:n.*86G>T
|
|
ENST00000596678.2:c.66G>T
|
ENSP00000470064.2:p.Val22=
|
|
NM_004278.3:c.492G>T
|
NP_004269.1:p.Val164=
|
|
XM_011524080.1:c.492G>T
|
XP_011522382.1:p.Val164=
|
|
XR_243571.2:n.510G>T
|
|
|
XR_429826.2:n.510G>T
|
|
|
XM_011524080.2:c.492G>T
|
XP_011522382.1:p.Val164=
|
|
XM_017025349.1:c.492G>T
|
XP_016880838.1:p.Val164=
|
|
XM_017025350.1:c.492G>T
|
XP_016880839.1:p.Val164=
|
|
XM_017025351.1:c.492G>T
|
XP_016880840.1:p.Val164=
|
|
XM_017025352.1:c.492G>T
|
XP_016880841.1:p.Val164=
|
|
XM_017025353.1:c.492G>T
|
XP_016880842.1:p.Val164=
|
|
XM_017025354.1:c.492G>T
|
XP_016880843.1:p.Val164=
|
|
XM_017025355.1:c.492G>T
|
XP_016880844.1:p.Val164=
|
|
XM_017025356.1:c.492G>T
|
XP_016880845.1:p.Val164=
|
|
NM_004278.4:c.492G>T
MANE Select
|
NP_004269.1:p.Val164=
|
|