ENST00000700029.2:c.-774T=
|
ENSP00000514759.2:n.-774T=
|
|
ENST00000710265.1:c.-774T=
|
ENSP00000518161.1:n.-774T=
|
|
ENST00000706954.1:c.-16-758T=
|
ENSP00000516674.1:n.-16-758T=
|
|
ENST00000706955.1:c.-774T=
|
ENSP00000516675.1:n.-774T=
|
|
ENST00000688158.1:c.-774T=
|
ENSP00000509254.1:n.-774T=
|
|
ENST00000688308.1:c.-17+583T=
|
ENSP00000508752.1:n.-17+583T=
|
|
ENST00000693560.1:c.-254T=
|
ENSP00000509861.1:n.-254T=
|
|
ENST00000371953.8:c.-774T=
MANE Select
|
ENSP00000361021.3:n.-774T=
|
|
ENST00000371953.7:c.-774T=
|
ENSP00000361021.3:n.-774T=
|
|
ENST00000610634.1:c.-876T=
|
ENSP00000477517.1:n.-876T=
|
|
NM_000314.5:c.-773T=
|
NP_000305.3:n.-773T=
|
|
NM_000314.6:c.-773T=
|
NP_000305.3:n.-773T=
|
|
NM_001304717.2:c.-254T=
|
NP_001291646.2:n.-254T=
|
|
NM_001304718.1:c.-1478T=
|
NP_001291647.1:n.-1478T=
|
|
NM_000314.7:c.-773T=
|
NP_000305.3:n.-773T=
|
|
NM_001304717.5:c.-254T=
|
NP_001291646.4:n.-254T=
|
|
NM_001304718.2:c.-1478T=
|
NP_001291647.1:n.-1478T=
|
|
NM_000314.8:c.-774T=
MANE Select
|
NP_000305.3:n.-774T=
|
|