ENST00000317276.9:c.2461+156T>A
MANE Select
|
ENSP00000314420.4:n.2461+156T>A
|
|
ENST00000317276.8:c.2461+156T>A
|
ENSP00000314420.4:n.2461+156T>A
|
|
ENST00000354903.9:c.2569T>A
|
ENSP00000346979.5:p.Ser857Thr
|
|
ENST00000578089.1:n.394+156T>A
|
|
|
ENST00000578950.1:n.420+156T>A
|
|
|
ENST00000581082.5:c.2392+165T>A
|
ENSP00000462064.1:n.2392+165T>A
|
|
ENST00000581395.5:c.*612T>A
|
ENSP00000464696.1:n.*612T>A
|
|
ENST00000582719.5:c.2461+156T>A
|
ENSP00000463054.1:n.2461+156T>A
|
|
ENST00000583559.1:c.310+156T>A
|
ENSP00000463369.1:n.310+156T>A
|
|
NM_002616.2:c.2461+156T>A
|
NP_002607.2:n.2461+156T>A
|
|
XM_005256689.1:c.2461+156T>A
|
XP_005256746.1:n.2461+156T>A
|
|
XM_005256690.1:c.2281+156T>A
|
XP_005256747.1:n.2281+156T>A
|
|
XM_005256689.2:c.2461+156T>A
|
XP_005256746.1:n.2461+156T>A
|
|
XM_024450803.1:c.2437T>A
|
XP_024306571.1:p.Ser813Thr
|
|
NM_002616.3:c.2461+156T>A
MANE Select
|
NP_002607.2:n.2461+156T>A
|
|