ENST00000267868.8:c.-77G>C
MANE Select
|
ENSP00000267868.3:n.-77G>C
|
|
ENST00000645673.2:c.-77G>C
|
ENSP00000493712.2:n.-77G>C
|
|
ENST00000267868.7:c.-77G>C
|
ENSP00000267868.3:n.-77G>C
|
|
ENST00000382643.7:c.-3+30G>C
|
ENSP00000372088.3:n.-3+30G>C
|
|
ENST00000423169.6:c.-77G>C
|
ENSP00000406602.2:n.-77G>C
|
|
ENST00000525066.5:c.-77G>C
|
ENSP00000431864.1:n.-77G>C
|
|
ENST00000527860.5:c.-3+531G>C
|
ENSP00000432759.1:n.-3+531G>C
|
|
ENST00000532743.5:c.-77G>C
|
ENSP00000433924.1:n.-77G>C
|
|
ENST00000557850.5:c.-77G>C
|
ENSP00000454176.1:n.-77G>C
|
|
NM_001164269.1:c.-3+30G>C
|
NP_001157741.1:n.-3+30G>C
|
|
NM_001164270.1:c.-77G>C
|
NP_001157742.1:n.-77G>C
|
|
NM_002875.4:c.-77G>C
|
NP_002866.2:n.-77G>C
|
|
NM_133487.3:c.-77G>C
|
NP_597994.3:n.-77G>C
|
|
XM_011521857.1:c.-3+531G>C
|
XP_011520159.1:n.-3+531G>C
|
|
XM_011521860.1:c.-3+30G>C
|
XP_011520162.1:n.-3+30G>C
|
|
XM_011521861.1:c.-3+531G>C
|
XP_011520163.1:n.-3+531G>C
|
|
XM_011521862.1:c.-331G>C
|
XP_011520164.1:n.-331G>C
|
|
XM_011521857.2:c.-3+531G>C
|
XP_011520159.1:n.-3+531G>C
|
|
XM_011521860.2:c.-3+30G>C
|
XP_011520162.1:n.-3+30G>C
|
|
XM_011521861.2:c.-3+531G>C
|
XP_011520163.1:n.-3+531G>C
|
|
XM_011521862.3:c.-331G>C
|
XP_011520164.1:n.-331G>C
|
|
NM_001164269.2:c.-3+30G>C
|
NP_001157741.1:n.-3+30G>C
|
|
NM_001164270.2:c.-77G>C
|
NP_001157742.1:n.-77G>C
|
|
NM_002875.5:c.-77G>C
MANE Select
|
NP_002866.2:n.-77G>C
|
|
NM_133487.4:c.-77G>C
|
NP_597994.3:n.-77G>C
|
|