ENST00000697337.1:c.*3092+407T>G
|
ENSP00000513259.1:n.*3092+407T>G
|
|
ENST00000697338.1:c.2276+335T>G
|
ENSP00000513260.1:n.2276+335T>G
|
|
ENST00000697339.1:c.1390+407T>G
|
ENSP00000513261.1:n.1390+407T>G
|
|
ENST00000697340.1:c.*1145+335T>G
|
ENSP00000513262.1:n.*1145+335T>G
|
|
ENST00000697341.1:n.2398+335T>G
|
|
|
ENST00000313735.11:c.2428+335T>G
MANE Select
|
ENSP00000327251.6:n.2428+335T>G
|
|
ENST00000646938.1:c.2425+335T>G
|
ENSP00000494870.1:n.2425+335T>G
|
|
ENST00000313735.10:c.2428+335T>G
|
ENSP00000327251.6:n.2428+335T>G
|
|
ENST00000621962.1:c.2311+335T>G
|
ENSP00000482291.1:n.2311+335T>G
|
|
NM_000625.4:c.2428+335T>G
MANE Select
|
NP_000616.3:n.2428+335T>G
|
|
XM_011524859.1:c.2428+335T>G
|
XP_011523161.1:n.2428+335T>G
|
|
XM_011524860.1:c.2425+335T>G
|
XP_011523162.1:n.2425+335T>G
|
|
XM_011524861.1:c.2356+407T>G
|
XP_011523163.1:n.2356+407T>G
|
|
XM_011524862.1:c.1762+335T>G
|
XP_011523164.1:n.1762+335T>G
|
|