ENST00000223051.8:c.1682+11G>T
MANE Select
|
ENSP00000223051.3:n.1682+11G>T
|
|
ENST00000223051.7:c.1682+11G>T
|
ENSP00000223051.3:n.1682+11G>T
|
|
ENST00000431692.5:c.*357+11G>T
|
ENSP00000413905.1:n.*357+11G>T
|
|
ENST00000462090.5:n.633+11G>T
|
|
|
ENST00000462107.1:c.1682+11G>T
|
ENSP00000420525.1:n.1682+11G>T
|
|
ENST00000465294.5:n.1517+11G>T
|
|
|
ENST00000473374.5:n.755+11G>T
|
|
|
ENST00000473963.1:n.711+11G>T
|
|
|
ENST00000476304.5:n.1303+11G>T
|
|
|
ENST00000490084.5:c.1035+11G>T
|
|
|
NM_001206855.1:c.1169+11G>T
|
NP_001193784.1:n.1169+11G>T
|
|
NM_003227.3:c.1682+11G>T
|
NP_003218.2:n.1682+11G>T
|
|
XM_005250553.3:c.1682+11G>T
|
XP_005250610.1:n.1682+11G>T
|
|
XM_005250554.3:c.1682+11G>T
|
XP_005250611.1:n.1682+11G>T
|
|
XR_927814.1:n.434-3423C>A
|
|
|
NM_001206855.2:c.1169+11G>T
|
NP_001193784.1:n.1169+11G>T
|
|
XM_005250553.4:c.1682+11G>T
|
XP_005250610.1:n.1682+11G>T
|
|
XM_017012573.1:c.1682+11G>T
|
XP_016868062.1:n.1682+11G>T
|
|
NM_003227.4:c.1682+11G>T
MANE Select
|
NP_003218.2:n.1682+11G>T
|
|
NM_001206855.3:c.1169+11G>T
|
NP_001193784.1:n.1169+11G>T
|
|