ENST00000366600.8:c.1369-2A>T
(B3GALNT2)
MANE Select
|
ENSP00000355559.3:n.1369-2A>T
|
|
ENST00000642610.2:c.*1580T>A
(TBCE)
MANE Select
|
ENSP00000494796.1:n.*1580T>A
|
|
ENST00000675193.1:c.*309-2A>T
(B3GALNT2)
|
ENSP00000502069.1:n.*309-2A>T
|
|
ENST00000675555.1:c.1147-2A>T
(B3GALNT2)
|
ENSP00000501896.1:n.1147-2A>T
|
|
ENST00000676288.1:c.*1015A>T
(B3GALNT2)
|
ENSP00000502392.1:n.*1015A>T
|
|
ENST00000366600.7:c.1369-2A>T
(B3GALNT2)
|
ENSP00000355559.3:n.1369-2A>T
|
|
NM_152490.4:c.1369-2A>T
(B3GALNT2)
|
NP_689703.1:n.1369-2A>T
|
|
XM_006711749.2:c.1369-2A>T
(B3GALNT2)
|
XP_006711812.1:n.1369-2A>T
|
|
XM_006711749.3:c.1369-2A>T
(B3GALNT2)
|
XP_006711812.1:n.1369-2A>T
|
|
XM_017000394.1:c.1492-2A>T
(B3GALNT2)
|
XP_016855883.1:n.1492-2A>T
|
|
XM_017000395.1:c.*45-2A>T
(B3GALNT2)
|
XP_016855884.1:n.*45-2A>T
|
|
XR_001736987.1:n.1473-2A>T
(B3GALNT2)
|
|
|
XR_001736989.1:n.1394-2A>T
(B3GALNT2)
|
|
|
XR_001736990.1:n.1356-2A>T
(B3GALNT2)
|
|
|
NM_003193.5:c.*1580T>A
(TBCE)
MANE Select
|
NP_003184.1:n.*1580T>A
|
|
NM_152490.5:c.1369-2A>T
(B3GALNT2)
MANE Select
|
NP_689703.1:n.1369-2A>T
|
|
NM_001079515.3:c.*1580T>A
(TBCE)
|
NP_001072983.1:n.*1580T>A
|
|
NM_001287801.2:c.*1580T>A
(TBCE)
|
NP_001274730.1:n.*1580T>A
|
|
NM_001287802.2:c.*1580T>A
(TBCE)
|
NP_001274731.1:n.*1580T>A
|
|