ENST00000553106.6:c.60+1G>A
MANE Select
|
ENSP00000448059.1:n.60+1G>A
|
|
ENST00000307000.7:c.-88+1G>A
|
ENSP00000303500.2:n.-88+1G>A
|
|
ENST00000546844.1:c.60+1G>A
|
ENSP00000446658.1:n.60+1G>A
|
|
ENST00000547319.1:n.371+1G>A
|
|
|
ENST00000549111.5:n.156+1G>A
|
|
|
ENST00000550978.6:c.44+1G>A
|
|
|
ENST00000551337.5:c.60+1G>A
|
ENSP00000447620.1:n.60+1G>A
|
|
ENST00000551988.5:n.149+1G>A
|
|
|
ENST00000553106.5:c.60+1G>A
|
ENSP00000448059.1:n.60+1G>A
|
|
ENST00000635500.1:n.29-4172G>A
|
|
|
NM_000277.1:c.60+1G>A
|
NP_000268.1:n.60+1G>A
|
|
XM_011538422.1:c.60+1G>A
|
XP_011536724.1:n.60+1G>A
|
|
NM_000277.2:c.60+1G>A
|
NP_000268.1:n.60+1G>A
|
|
NM_001354304.1:c.60+1G>A
|
NP_001341233.1:n.60+1G>A
|
|
XM_017019370.2:c.60+1G>A
|
XP_016874859.1:n.60+1G>A
|
|
NM_000277.3:c.60+1G>A
MANE Select
|
NP_000268.1:n.60+1G>A
|
|
NM_001354304.2:c.60+1G>A
|
NP_001341233.1:n.60+1G>A
|
|