|
NM_000969.5:c.3+13C>T
MANE Select
|
NP_000960.2:n.3+13C>T
|
|
ENST00000370321.8:c.3+13C>T
MANE Select
|
ENSP00000359345.2:n.3+13C>T
|
|
NM_000969.3:c.3+13C>T
|
NP_000960.2:n.3+13C>T
|
|
NR_146333.1:n.132+13C>T
|
|
|
ENST00000315741.5:c.-269C>T
|
ENSP00000359338.2:n.-269C>T
|
|
ENST00000370321.7:c.3+13C>T
|
ENSP00000359345.2:n.3+13C>T
|
|
ENST00000470843.5:c.3+13C>T
|
ENSP00000473675.1:n.3+13C>T
|
|
ENST00000645119.1:c.3+13C>T
|
ENSP00000493811.1:n.3+13C>T
|
|
ENST00000645300.1:c.-78+13C>T
|
ENSP00000495589.1:n.-78+13C>T
|
|
ENST00000646852.1:n.32+13C>T
|
|