|
ENST00000477750.6:n.2070+2T>A
(NAA10)
|
|
|
|
ENST00000700299.1:n.1723+2T>A
(NAA10)
|
|
|
|
ENST00000464845.6:c.471+2T>A
(NAA10)
MANE Select
|
ENSP00000417763.1:n.471+2T>A
|
|
|
ENST00000370009.5:c.426+2T>A
(NAA10)
|
ENSP00000359026.1:n.426+2T>A
|
|
|
ENST00000370011.7:c.408+2T>A
(NAA10)
|
ENSP00000359028.3:n.408+2T>A
|
|
|
ENST00000370015.8:c.471+2T>A
(NAA10)
|
ENSP00000359032.4:n.471+2T>A
|
|
|
ENST00000393712.7:c.471+2T>A
(NAA10)
|
ENSP00000377315.3:n.471+2T>A
|
|
|
ENST00000460996.5:n.760+2T>A
(NAA10)
|
|
|
|
ENST00000464845.5:c.471+2T>A
(NAA10)
|
ENSP00000417763.1:n.471+2T>A
|
|
|
ENST00000466877.5:n.782+2T>A
(NAA10)
|
|
|
|
ENST00000467451.1:n.275T>A
(NAA10)
|
|
|
|
ENST00000482485.1:n.678+2T>A
(NAA10)
|
|
|
|
ENST00000484950.5:n.690+2T>A
(NAA10)
|
|
|
|
ENST00000494813.5:n.481+1310T>A
(ARHGAP4)
|
|
|
|
NM_001256119.1:c.426+2T>A
(NAA10)
|
NP_001243048.1:n.426+2T>A
|
|
|
NM_001256120.1:c.453+2T>A
(NAA10)
|
NP_001243049.1:n.453+2T>A
|
|
|
NM_003491.3:c.471+2T>A
(NAA10)
|
NP_003482.1:n.471+2T>A
|
|
|
NM_003491.4:c.471+2T>A
(NAA10)
MANE Select
|
NP_003482.1:n.471+2T>A
|
|
|
NM_001256119.2:c.426+2T>A
(NAA10)
|
NP_001243048.1:n.426+2T>A
|
|
|
NM_001256120.2:c.453+2T>A
(NAA10)
|
NP_001243049.1:n.453+2T>A
|
|
