ENST00000369458.8:c.32+2081G>A
MANE Select
|
ENSP00000358470.3:n.32+2081G>A
|
|
ENST00000328189.7:c.32+2081G>A
|
ENSP00000328168.3:n.32+2081G>A
|
|
ENST00000369458.7:c.32+2081G>A
|
ENSP00000358470.3:n.32+2081G>A
|
|
ENST00000430871.3:c.32+2081G>A
|
ENSP00000484316.1:n.32+2081G>A
|
|
ENST00000463461.5:n.104+2081G>A
|
|
|
NM_001253850.1:c.32+2081G>A
|
NP_001240779.1:n.32+2081G>A
|
|
NM_024626.3:c.32+2081G>A
|
NP_078902.2:n.32+2081G>A
|
|
NR_045603.1:n.137+2081G>A
|
|
|
NR_045604.1:n.137+2081G>A
|
|
|
XM_011542144.1:c.87-38572G>A
|
XP_011540446.1:n.87-38572G>A
|
|
XM_017002335.2:c.-232+2081G>A
|
XP_016857824.1:n.-232+2081G>A
|
|
NM_024626.4:c.32+2081G>A
MANE Select
|
NP_078902.2:n.32+2081G>A
|
|
NR_045603.2:n.104+2081G>A
|
|
|
NR_045604.2:n.104+2081G>A
|
|
|
NM_001253850.2:c.32+2081G>A
|
NP_001240779.1:n.32+2081G>A
|
|