ENST00000393597.7:c.-199-4298G>T
MANE Select
|
ENSP00000377222.2:n.-199-4298G>T
|
|
ENST00000311131.6:c.-333-4298G>T
|
ENSP00000310305.2:n.-333-4298G>T
|
|
ENST00000393596.2:c.-199-4298G>T
|
ENSP00000377221.2:n.-199-4298G>T
|
|
ENST00000393597.6:c.-199-4298G>T
|
ENSP00000377222.2:n.-199-4298G>T
|
|
NM_002564.3:c.-199-4298G>T
|
NP_002555.3:n.-199-4298G>T
|
|
NM_176071.2:c.-199-4298G>T
|
NP_788085.2:n.-199-4298G>T
|
|
NM_176072.2:c.-333-4298G>T
|
NP_788086.2:n.-333-4298G>T
|
|
XM_005274019.3:c.-199-4298G>T
|
XP_005274076.1:n.-199-4298G>T
|
|
XM_005274020.3:c.-200+3064G>T
|
XP_005274077.1:n.-200+3064G>T
|
|
XM_005274021.3:c.-199-4298G>T
|
XP_005274078.1:n.-199-4298G>T
|
|
XM_011545074.1:c.-199-4298G>T
|
XP_011543376.1:n.-199-4298G>T
|
|
XM_005274019.4:c.-199-4298G>T
|
XP_005274076.1:n.-199-4298G>T
|
|
XM_005274020.4:c.-200+3064G>T
|
XP_005274077.1:n.-200+3064G>T
|
|
XM_005274021.4:c.-199-4298G>T
|
XP_005274078.1:n.-199-4298G>T
|
|
XM_011545074.2:c.-199-4298G>T
|
XP_011543376.1:n.-199-4298G>T
|
|
XM_017017839.1:c.-199-4298G>T
|
XP_016873328.1:n.-199-4298G>T
|
|
XR_001747890.1:n.154-4298G>T
|
|
|
XR_001747891.1:n.154-4298G>T
|
|
|
XR_001747892.1:n.154-4298G>T
|
|
|
NM_002564.4:c.-199-4298G>T
MANE Select
|
NP_002555.4:n.-199-4298G>T
|
|
NM_176071.3:c.-199-4298G>T
|
NP_788085.3:n.-199-4298G>T
|
|
NM_176072.3:c.-333-4298G>T
|
NP_788086.3:n.-333-4298G>T
|
|