ENST00000233627.14:c.408+1G>T
MANE Select
|
ENSP00000233627.9:n.408+1G>T
|
|
ENST00000233627.13:c.408+1G>T
|
ENSP00000233627.9:n.408+1G>T
|
|
ENST00000313408.11:c.408+1G>T
|
ENSP00000364262.5:n.408+1G>T
|
|
ENST00000414651.3:c.498+1G>T
|
ENSP00000406630.2:n.498+1G>T
|
|
ENST00000436115.6:n.2363+1G>T
|
|
|
ENST00000534853.5:c.*202+1G>T
|
ENSP00000442822.1:n.*202+1G>T
|
|
ENST00000535382.1:n.660+1G>T
|
|
|
ENST00000538523.5:n.464+1G>T
|
|
|
ENST00000538662.5:n.436G>T
|
|
|
ENST00000538929.5:n.498+1G>T
|
|
|
ENST00000539480.5:c.408+1G>T
|
ENSP00000443273.1:n.408+1G>T
|
|
ENST00000540530.5:n.399+1G>T
|
|
|
ENST00000543289.5:n.899G>T
|
|
|
ENST00000545446.5:n.699+1G>T
|
|
|
ENST00000546172.7:c.*404+1G>T
|
ENSP00000467094.1:n.*404+1G>T
|
|
ENST00000546283.5:c.408+1G>T
|
ENSP00000440348.1:n.408+1G>T
|
|
ENST00000618074.4:c.408+1G>T
|
ENSP00000477895.1:n.408+1G>T
|
|
ENST00000620479.4:c.408+1G>T
|
ENSP00000480984.1:n.408+1G>T
|
|
ENST00000622587.4:n.405G>T
|
|
|
NM_024407.4:c.408+1G>T
|
NP_077718.3:n.408+1G>T
|
|
XM_005259556.3:c.408+1G>T
|
XP_005259613.2:n.408+1G>T
|
|
NM_001363602.1:c.408+1G>T
|
NP_001350531.1:n.408+1G>T
|
|
XM_024451499.1:c.429+1G>T
|
XP_024307267.1:n.429+1G>T
|
|
NM_024407.5:c.408+1G>T
MANE Select
|
NP_077718.3:n.408+1G>T
|
|
NM_001363602.2:c.408+1G>T
|
NP_001350531.1:n.408+1G>T
|
|