ENST00000599547.6:c.10973+20G>T
|
ENSP00000471601.2:n.10973+20G>T
|
|
ENST00000359596.8:c.11034+20G>T
MANE Select
|
ENSP00000352608.2:n.11034+20G>T
|
|
ENST00000355481.8:c.11019+20G>T
|
ENSP00000347667.3:n.11019+20G>T
|
|
ENST00000359596.7:c.11034+20G>T
|
ENSP00000352608.2:n.11034+20G>T
|
|
ENST00000360985.7:c.11016+20G>T
|
ENSP00000354254.4:n.11016+20G>T
|
|
ENST00000594335.5:c.4421+20G>T
|
|
|
ENST00000599547.5:c.1841+20G>T
|
|
|
ENST00000601514.5:c.315+20G>T
|
ENSP00000472497.1:n.315+20G>T
|
|
NM_000540.2:c.11034+20G>T , LRG_766t1:c.11034+20G>T
|
NP_000531.2:n.11034+20G>T
|
|
NM_001042723.1:c.11019+20G>T
|
NP_001036188.1:n.11019+20G>T
|
|
XM_006723317.1:c.11034+20G>T
|
XP_006723380.1:n.11034+20G>T
|
|
XM_006723319.1:c.11019+20G>T
|
XP_006723382.1:n.11019+20G>T
|
|
XM_011527204.1:c.11031+20G>T
|
XP_011525506.1:n.11031+20G>T
|
|
XM_011527205.1:c.11034+20G>T
|
XP_011525507.1:n.11034+20G>T
|
|
XM_006723317.2:c.11034+20G>T
|
XP_006723380.1:n.11034+20G>T
|
|
XM_006723319.2:c.11019+20G>T
|
XP_006723382.1:n.11019+20G>T
|
|
XM_011527205.2:c.11034+20G>T
|
XP_011525507.1:n.11034+20G>T
|
|
NM_000540.3:c.11034+20G>T
MANE Select
|
NP_000531.2:n.11034+20G>T
|
|
NM_001042723.2:c.11019+20G>T
|
NP_001036188.1:n.11019+20G>T
|
|