|
NM_016292.3:c.1165+5G>A
(TRAP1)
MANE Select
|
NP_057376.2:n.1165+5G>A
|
|
ENST00000246957.10:c.1165+5G>A
(TRAP1)
MANE Select
|
ENSP00000246957.5:n.1165+5G>A
|
|
NM_001272049.1:c.1006+5G>A
(TRAP1)
|
NP_001258978.1:n.1006+5G>A
|
|
NM_001272049.2:c.1006+5G>A
(TRAP1)
|
NP_001258978.1:n.1006+5G>A
|
|
NM_016292.2:c.1165+5G>A
(TRAP1)
|
NP_057376.2:n.1165+5G>A
|
|
ENST00000246957.9:c.1165+5G>A
(TRAP1)
|
ENSP00000246957.5:n.1165+5G>A
|
|
ENST00000538171.5:c.1006+5G>A
(TRAP1)
|
ENSP00000442070.1:n.1006+5G>A
|
|
ENST00000573872.5:n.494-904G>A
(TRAP1)
|
|
|
ENST00000575479.1:c.219-7054C>T
(DNASE1)
|
|
|
ENST00000575671.5:c.538+5G>A
(TRAP1)
|
ENSP00000458166.1:n.538+5G>A
|
|
ENST00000576335.5:c.538+5G>A
(TRAP1)
|
ENSP00000459354.1:n.538+5G>A
|
|
XM_011522345.1:c.745+5G>A
(TRAP1)
|
XP_011520647.1:n.745+5G>A
|
|
XM_011522345.2:c.745+5G>A
(TRAP1)
|
XP_011520647.1:n.745+5G>A
|