ENST00000698254.1:c.-5+606G>T
|
ENSP00000513629.1:n.-5+606G>T
|
|
ENST00000698255.1:c.-5+606G>T
|
ENSP00000513630.1:n.-5+606G>T
|
|
ENST00000265686.8:c.-5+606G>T
MANE Select
|
ENSP00000265686.3:n.-5+606G>T
|
|
ENST00000265686.7:c.-5+606G>T
|
ENSP00000265686.3:n.-5+606G>T
|
|
ENST00000524598.5:c.-5+606G>T
|
ENSP00000432846.1:n.-5+606G>T
|
|
ENST00000529657.1:c.-175-67G>T
|
ENSP00000435023.1:n.-175-67G>T
|
|
ENST00000533947.1:n.5+606G>T
|
|
|
ENST00000534673.5:c.-5+606G>T
|
ENSP00000431174.1:n.-5+606G>T
|
|
NM_006019.3:c.-5+606G>T
|
NP_006010.2:n.-5+606G>T
|
|
XM_005273709.2:c.-175-67G>T
|
XP_005273766.1:n.-175-67G>T
|
|
NM_001351059.1:c.-1254+606G>T
|
NP_001337988.1:n.-1254+606G>T
|
|
XM_024448320.1:c.-5+606G>T
|
XP_024304088.1:n.-5+606G>T
|
|
XM_024448321.1:c.-175-67G>T
|
XP_024304089.1:n.-175-67G>T
|
|
XM_024448323.1:c.-5+606G>T
|
XP_024304091.1:n.-5+606G>T
|
|
XM_024448324.1:c.-5+606G>T
|
XP_024304092.1:n.-5+606G>T
|
|
XR_001747721.2:n.120+606G>T
|
|
|
XR_001747722.1:n.117+606G>T
|
|
|
XR_001747723.2:n.117+606G>T
|
|
|
XR_002957115.1:n.118+606G>T
|
|
|
NM_006019.4:c.-5+606G>T
MANE Select
|
NP_006010.2:n.-5+606G>T
|
|
NM_001351059.2:c.-1254+606G>T
|
NP_001337988.1:n.-1254+606G>T
|
|