|
NM_000154.2:c.475+1G>A
MANE Select
|
NP_000145.1:n.475+1G>A
|
|
ENST00000588479.6:c.475+1G>A
MANE Select
|
ENSP00000465930.1:n.475+1G>A
|
|
NM_000154.1:c.475+1G>A
|
NP_000145.1:n.475+1G>A
|
|
NM_001381985.1:c.475+1G>A
|
NP_001368914.1:n.475+1G>A
|
|
ENST00000225614.6:c.475+1G>A
|
ENSP00000225614.1:n.475+1G>A
|
|
ENST00000586244.1:c.*200G>A
|
ENSP00000468288.1:n.*200G>A
|
|
ENST00000587707.1:c.229+1G>A
|
ENSP00000468341.1:n.229+1G>A
|
|
ENST00000587707.2:c.475+1G>A
|
ENSP00000468341.2:n.475+1G>A
|
|
ENST00000588479.5:c.475+1G>A
|
ENSP00000465930.1:n.475+1G>A
|
|
ENST00000592494.1:n.497G>A
|
|
|
ENST00000592997.6:c.475+1G>A
|
ENSP00000464765.2:n.475+1G>A
|