ENST00000356487.11:c.1474+1G>T
MANE Select
|
ENSP00000348877.3:n.1474+1G>T
|
|
ENST00000415930.8:c.1591+1G>T
|
ENSP00000405573.3:n.1591+1G>T
|
|
ENST00000586425.2:c.1158-104G>T
|
|
|
ENST00000588991.7:c.1507+1G>T
|
ENSP00000465858.3:n.1507+1G>T
|
|
ENST00000643067.1:n.2519+1G>T
|
|
|
ENST00000647446.1:c.*525+1G>T
|
ENSP00000495129.1:n.*525+1G>T
|
|
ENST00000356487.9:c.1474+1G>T
|
ENSP00000348877.3:n.1474+1G>T
|
|
ENST00000415930.7:c.1507+1G>T
|
ENSP00000405573.2:n.1507+1G>T
|
|
ENST00000586077.1:n.2350G>T
|
|
|
ENST00000586392.1:n.1212+1G>T
|
|
|
ENST00000586425.1:c.1399-269G>T
|
ENSP00000467670.2:n.1399-269G>T
|
|
ENST00000588991.6:c.1519+1G>T
|
ENSP00000465858.2:n.1519+1G>T
|
|
ENST00000592740.5:c.193+2975G>T
|
|
|
NM_000175.3:c.1474+1G>T
|
NP_000166.2:n.1474+1G>T
|
|
NM_001184722.1:c.1507+1G>T
|
NP_001171651.1:n.1507+1G>T
|
|
NM_001289789.1:c.1591+1G>T
|
NP_001276718.1:n.1591+1G>T
|
|
NM_001289790.1:c.1390+1G>T
|
NP_001276719.1:n.1390+1G>T
|
|
XM_005258764.1:c.1474+1G>T
|
XP_005258821.1:n.1474+1G>T
|
|
XM_006723148.1:c.1474+1G>T
|
XP_006723211.1:n.1474+1G>T
|
|
XM_011526754.1:c.1591+1G>T
|
XP_011525056.1:n.1591+1G>T
|
|
NM_000175.5:c.1474+1G>T
MANE Select
|
NP_000166.2:n.1474+1G>T
|
|
NM_001289790.2:c.1390+1G>T
|
NP_001276719.1:n.1390+1G>T
|
|
NM_001329909.1:c.1474+1G>T
|
NP_001316838.1:n.1474+1G>T
|
|
NM_001329910.1:c.1474+1G>T
|
NP_001316839.1:n.1474+1G>T
|
|
NM_001329911.1:c.1447+1G>T
|
NP_001316840.1:n.1447+1G>T
|
|
XM_011526754.3:c.1591+1G>T
|
XP_011525056.1:n.1591+1G>T
|
|
NM_001289790.3:c.1390+1G>T
|
NP_001276719.1:n.1390+1G>T
|
|
NM_001329911.2:c.1447+1G>T
|
NP_001316840.1:n.1447+1G>T
|
|