ENST00000326828.6:c.*719T>A
MANE Select
|
ENSP00000315602.5:n.*719T>A
|
|
ENST00000326828.5:c.*719T>A
|
ENSP00000315602.5:n.*719T>A
|
|
ENST00000348639.7:c.1390-2694T>A
|
ENSP00000267951.4:n.1390-2694T>A
|
|
ENST00000559002.5:n.193+655T>A
|
|
|
ENST00000559658.5:c.*64+655T>A
|
ENSP00000452896.1:n.*64+655T>A
|
|
NM_000743.4:c.*719T>A
|
NP_000734.2:n.*719T>A
|
|
NM_001166694.1:c.1390-2694T>A
|
NP_001160166.1:n.1390-2694T>A
|
|
NR_046313.1:n.2083+655T>A
|
|
|
XM_006720382.1:c.*719T>A
|
XP_006720445.1:n.*719T>A
|
|
XM_011521173.1:c.*719T>A
|
XP_011519475.1:n.*719T>A
|
|
XM_006720382.3:c.*719T>A
|
XP_006720445.1:n.*719T>A
|
|
NM_000743.5:c.*719T>A
MANE Select
|
NP_000734.2:n.*719T>A
|
|
NM_001166694.2:c.1390-2694T>A
|
NP_001160166.1:n.1390-2694T>A
|
|
NR_046313.2:n.1784+655T>A
|
|
|