ENST00000404085.7:c.460+5G>T
MANE Select
|
ENSP00000384008.3:n.460+5G>T
|
|
ENST00000404261.9:c.460+5G>T
|
ENSP00000384753.6:n.460+5G>T
|
|
ENST00000594072.6:c.460+5G>T
|
ENSP00000468845.4:n.460+5G>T
|
|
ENST00000651416.1:n.677+5G>T
|
|
|
ENST00000652132.1:c.427+5G>T
|
ENSP00000498416.1:n.427+5G>T
|
|
ENST00000394458.7:c.622+5G>T
|
ENSP00000377971.4:n.622+5G>T
|
|
ENST00000404085.5:c.*359+5G>T
|
ENSP00000384008.2:n.*359+5G>T
|
|
ENST00000404261.8:c.622+5G>T
|
ENSP00000384753.5:n.622+5G>T
|
|
ENST00000594072.5:c.622+5G>T
|
ENSP00000468845.3:n.622+5G>T
|
|
ENST00000596099.1:n.366G>T
|
|
|
ENST00000596626.1:n.573+5G>T
|
|
|
ENST00000596834.1:n.513G>T
|
|
|
ENST00000598347.2:c.462+5G>T
|
|
|
NM_001278443.1:c.589+5G>T
|
NP_001265372.1:n.589+5G>T
|
|
NM_001278444.1:c.622+5G>T
|
NP_001265373.1:n.622+5G>T
|
|
NM_001278445.1:c.526+5G>T
|
NP_001265374.1:n.526+5G>T
|
|
NM_152363.5:c.622+5G>T
|
NP_689576.5:n.622+5G>T
|
|
NR_103530.1:n.736+5G>T
|
|
|
NM_001278443.2:c.427+5G>T
|
NP_001265372.2:n.427+5G>T
|
|
NM_001278444.2:c.460+5G>T
|
NP_001265373.2:n.460+5G>T
|
|
NM_001278445.2:c.418+5G>T
|
NP_001265374.2:n.418+5G>T
|
|
NM_152363.6:c.460+5G>T
MANE Select
|
NP_689576.6:n.460+5G>T
|
|
NR_103530.2:n.480+5G>T
|
|
|