ENST00000329597.12:c.-7A>T
MANE Select
|
ENSP00000333203.7:n.-7A>T
|
|
ENST00000329597.11:c.-7A>T
|
ENSP00000333203.7:n.-7A>T
|
|
ENST00000553511.1:c.-7A>T
|
ENSP00000451215.1:n.-7A>T
|
|
ENST00000553780.5:c.-7A>T
|
ENSP00000450837.1:n.-7A>T
|
|
ENST00000554220.5:c.-7A>T
|
ENSP00000450484.1:n.-7A>T
|
|
ENST00000554276.1:c.-7A>T
|
ENSP00000451610.1:n.-7A>T
|
|
ENST00000554633.5:c.-7A>T
|
ENSP00000451697.1:n.-7A>T
|
|
ENST00000554760.5:c.-7A>T
|
ENSP00000452469.1:n.-7A>T
|
|
ENST00000554866.5:c.-7A>T
|
ENSP00000451126.1:n.-7A>T
|
|
ENST00000555681.1:c.-7A>T
|
ENSP00000451650.1:n.-7A>T
|
|
ENST00000556064.1:c.-7A>T
|
ENSP00000451487.1:n.-7A>T
|
|
ENST00000556730.1:n.111A>T
|
|
|
ENST00000556775.5:c.-7A>T
|
ENSP00000450745.1:n.-7A>T
|
|
ENST00000557598.1:c.-7A>T
|
ENSP00000450485.1:n.-7A>T
|
|
NM_000624.5:c.-7A>T
|
NP_000615.3:n.-7A>T
|
|
NM_000624.6:c.-7A>T
MANE Select
|
NP_000615.3:n.-7A>T
|
|