ENST00000373713.7:c.-13G>T
MANE Select
|
ENSP00000362817.2:n.-13G>T
|
|
ENST00000373713.6:c.-13G>T
|
ENSP00000362817.2:n.-13G>T
|
|
ENST00000482018.1:c.-13G>T
|
ENSP00000473982.1:n.-13G>T
|
|
ENST00000498148.5:c.-13G>T
|
ENSP00000474078.1:n.-13G>T
|
|
NM_004102.3:c.-13G>T
|
NP_004093.1:n.-13G>T
|
|
XM_011541007.1:c.-13G>T
|
XP_011539309.1:n.-13G>T
|
|
NM_001320996.1:c.-13G>T
|
NP_001307925.1:n.-13G>T
|
|
NM_004102.4:c.-13G>T
|
NP_004093.1:n.-13G>T
|
|
XM_011541007.3:c.-13G>T
|
XP_011539309.1:n.-13G>T
|
|
NM_004102.5:c.-13G>T
MANE Select
|
NP_004093.1:n.-13G>T
|
|
NM_001320996.2:c.-13G>T
|
NP_001307925.1:n.-13G>T
|
|