ENST00000261674.9:c.1454+362G>A
MANE Select
|
ENSP00000261674.4:n.1454+362G>A
|
|
ENST00000261674.8:c.1454+362G>A
|
ENSP00000261674.4:n.1454+362G>A
|
|
ENST00000535236.5:n.4788+362G>A
|
|
|
ENST00000537164.1:c.373+362G>A
|
|
|
ENST00000538548.5:c.*1041+362G>A
|
ENSP00000445832.1:n.*1041+362G>A
|
|
ENST00000541286.5:c.1454+362G>A
|
ENSP00000437738.1:n.1454+362G>A
|
|
NM_001261411.1:c.1454+362G>A
|
NP_001248340.1:n.1454+362G>A
|
|
NM_004592.3:c.1454+362G>A
|
NP_004583.2:n.1454+362G>A
|
|
XM_011538653.1:c.1454+362G>A
|
XP_011536955.1:n.1454+362G>A
|
|
XM_011538654.1:c.1076+362G>A
|
XP_011536956.1:n.1076+362G>A
|
|
XM_011538655.1:c.1454+362G>A
|
XP_011536957.1:n.1454+362G>A
|
|
XM_011538654.2:c.1076+362G>A
|
XP_011536956.1:n.1076+362G>A
|
|
XM_011538655.2:c.1454+362G>A
|
XP_011536957.1:n.1454+362G>A
|
|
XM_017019798.1:c.1454+362G>A
|
XP_016875287.1:n.1454+362G>A
|
|
XM_017019799.1:c.833+362G>A
|
XP_016875288.1:n.833+362G>A
|
|
XM_024449125.1:c.1076+362G>A
|
XP_024304893.1:n.1076+362G>A
|
|
XM_024449126.1:c.1076+362G>A
|
XP_024304894.1:n.1076+362G>A
|
|
NM_001261411.2:c.1454+362G>A
|
NP_001248340.1:n.1454+362G>A
|
|
NM_004592.4:c.1454+362G>A
MANE Select
|
NP_004583.2:n.1454+362G>A
|
|