ENST00000563236.6:c.2924+324G>T
MANE Select
|
ENSP00000456149.2:n.2924+324G>T
|
|
ENST00000262502.5:c.2921+324G>T
|
ENSP00000262502.5:n.2921+324G>T
|
|
ENST00000438926.6:c.2951+324G>T
|
ENSP00000402152.2:n.2951+324G>T
|
|
ENST00000563236.5:c.2924+324G>T
|
ENSP00000456149.1:n.2924+324G>T
|
|
ENST00000566786.5:c.2948+324G>T
|
ENSP00000457552.1:n.2948+324G>T
|
|
ENST00000569002.1:n.679G>T
|
|
|
NM_000339.2:c.2951+324G>T
|
NP_000330.2:n.2951+324G>T
|
|
NM_001126107.1:c.2948+324G>T
|
NP_001119579.1:n.2948+324G>T
|
|
NM_001126108.1:c.2924+324G>T
|
NP_001119580.1:n.2924+324G>T
|
|
XM_005256119.1:c.2921+324G>T
|
XP_005256176.1:n.2921+324G>T
|
|
XM_005256119.2:c.2921+324G>T
|
XP_005256176.1:n.2921+324G>T
|
|
NM_000339.3:c.2951+324G>T
|
NP_000330.3:n.2951+324G>T
|
|
NM_001126107.2:c.2948+324G>T
|
NP_001119579.2:n.2948+324G>T
|
|
NM_001126108.2:c.2924+324G>T
MANE Select
|
NP_001119580.2:n.2924+324G>T
|
|