ENST00000477151.2:n.303+69G>A
|
|
|
ENST00000643794.1:c.236+69G>A
|
ENSP00000495765.1:n.236+69G>A
|
|
ENST00000651669.1:c.115+69G>A
MANE Select
|
ENSP00000499044.1:n.115+69G>A
|
|
ENST00000368567.4:c.115+69G>A
|
ENSP00000357555.4:n.115+69G>A
|
|
ENST00000392558.4:c.184G>A
|
ENSP00000376341.4:p.Ala62Thr
|
|
ENST00000477151.1:n.270+69G>A
|
|
|
ENST00000493224.5:n.381+69G>A
|
|
|
NM_001030.4:c.115+69G>A
|
NP_001021.1:n.115+69G>A
|
|
NM_001030.6:c.115+69G>A
MANE Select
|
NP_001021.1:n.115+69G>A
|
|
NM_001349946.1:c.19+69G>A
|
NP_001336875.1:n.19+69G>A
|
|
NM_001349947.1:c.19+69G>A
|
NP_001336876.1:n.19+69G>A
|
|
NM_001349946.2:c.19+69G>A
|
NP_001336875.1:n.19+69G>A
|
|
NM_001349947.2:c.19+69G>A
|
NP_001336876.1:n.19+69G>A
|
|