ENST00000257904.11:c.522+49G>T
MANE Select
|
ENSP00000257904.5:n.522+49G>T
|
|
ENST00000257904.10:c.522+49G>T
|
ENSP00000257904.5:n.522+49G>T
|
|
ENST00000312990.10:c.265-203G>T
|
ENSP00000316889.6:n.265-203G>T
|
|
ENST00000546489.5:c.300+49G>T
|
ENSP00000447779.1:n.300+49G>T
|
|
ENST00000547281.5:c.300+49G>T
|
ENSP00000447274.1:n.300+49G>T
|
|
ENST00000549606.5:c.-158+1301G>T
|
ENSP00000447005.1:n.-158+1301G>T
|
|
ENST00000550419.5:c.522+49G>T
|
ENSP00000448098.1:n.522+49G>T
|
|
ENST00000551706.1:n.937G>T
|
|
|
ENST00000551800.5:c.300+49G>T
|
ENSP00000449391.1:n.300+49G>T
|
|
ENST00000551888.5:n.443-203G>T
|
|
|
ENST00000552254.5:c.522+49G>T
|
ENSP00000449179.1:n.522+49G>T
|
|
ENST00000553237.5:c.*161+49G>T
|
ENSP00000448885.1:n.*161+49G>T
|
|
NM_000075.3:c.522+49G>T
|
NP_000066.1:n.522+49G>T
|
|
NM_000075.4:c.522+49G>T
MANE Select
|
NP_000066.1:n.522+49G>T
|
|