ENST00000477151.2:n.303+11G>T
|
|
|
ENST00000643794.1:c.236+11G>T
|
ENSP00000495765.1:n.236+11G>T
|
|
ENST00000651669.1:c.115+11G>T
MANE Select
|
ENSP00000499044.1:n.115+11G>T
|
|
ENST00000368567.4:c.115+11G>T
|
ENSP00000357555.4:n.115+11G>T
|
|
ENST00000392558.4:c.126G>T
|
ENSP00000376341.4:p.Thr42=
|
|
ENST00000477151.1:n.270+11G>T
|
|
|
ENST00000493224.5:n.381+11G>T
|
|
|
NM_001030.4:c.115+11G>T
|
NP_001021.1:n.115+11G>T
|
|
NM_001030.6:c.115+11G>T
MANE Select
|
NP_001021.1:n.115+11G>T
|
|
NM_001349946.1:c.19+11G>T
|
NP_001336875.1:n.19+11G>T
|
|
NM_001349947.1:c.19+11G>T
|
NP_001336876.1:n.19+11G>T
|
|
NM_001349946.2:c.19+11G>T
|
NP_001336875.1:n.19+11G>T
|
|
NM_001349947.2:c.19+11G>T
|
NP_001336876.1:n.19+11G>T
|
|