ENST00000395925.8:c.-52G>T
MANE Select
|
ENSP00000379258.3:n.-52G>T
|
|
ENST00000428534.2:c.-43+804G>T
|
ENSP00000503957.1:n.-43+804G>T
|
|
ENST00000677605.1:c.-43+519G>T
|
ENSP00000503743.1:n.-43+519G>T
|
|
ENST00000677990.1:n.230G>T
|
|
|
ENST00000678978.1:c.-42-13685G>T
|
ENSP00000503352.1:n.-42-13685G>T
|
|
ENST00000395925.7:c.-52G>T
|
ENSP00000379258.3:n.-52G>T
|
|
ENST00000428534.1:n.87+804G>T
|
|
|
ENST00000437480.1:c.-52G>T
|
ENSP00000407963.1:n.-52G>T
|
|
NM_000168.5:c.-52G>T
|
NP_000159.3:n.-52G>T
|
|
XM_005249703.1:c.-43+804G>T
|
XP_005249760.1:n.-43+804G>T
|
|
XM_005249704.2:c.-43+519G>T
|
XP_005249761.1:n.-43+519G>T
|
|
XM_011515273.1:c.-42-13685G>T
|
XP_011513575.1:n.-42-13685G>T
|
|
NM_000168.6:c.-52G>T
MANE Select
|
NP_000159.3:n.-52G>T
|
|