|
ENST00000356839.10:c.1827+1G>A
MANE Select
|
ENSP00000349297.5:n.1827+1G>A
|
|
|
ENST00000322910.9:c.*1782+1G>A
|
ENSP00000325395.5:n.*1782+1G>A
|
|
|
ENST00000350303.9:c.1761+1G>A
|
ENSP00000344152.5:n.1761+1G>A
|
|
|
ENST00000356839.9:c.1827+1G>A
|
ENSP00000349297.5:n.1827+1G>A
|
|
|
ENST00000542255.6:c.706+1G>A
|
|
|
|
ENST00000543245.6:c.1896+1G>A
|
ENSP00000438689.2:n.1896+1G>A
|
|
|
ENST00000578033.1:n.252+1G>A
|
|
|
|
ENST00000578319.5:n.408+1G>A
|
|
|
|
ENST00000578711.1:n.1381G>A
|
|
|
|
ENST00000578809.5:n.399+1G>A
|
|
|
|
ENST00000579425.5:n.943+1G>A
|
|
|
|
ENST00000579546.1:c.562+1G>A
|
|
|
|
ENST00000583848.5:c.193+1G>A
|
ENSP00000466487.1:n.193+1G>A
|
|
|
ENST00000583850.5:n.598+1G>A
|
|
|
|
ENST00000583858.5:c.758+1G>A
|
|
|
|
NM_000018.3:c.1827+1G>A
|
NP_000009.1:n.1827+1G>A
|
|
|
NM_001033859.2:c.1761+1G>A
|
NP_001029031.1:n.1761+1G>A
|
|
|
NM_001270447.1:c.1896+1G>A
|
NP_001257376.1:n.1896+1G>A
|
|
|
NM_001270448.1:c.1599+1G>A
|
NP_001257377.1:n.1599+1G>A
|
|
|
XM_006721516.2:c.1848+1G>A
|
XP_006721579.2:n.1848+1G>A
|
|
|
XM_011523829.1:c.1746+1G>A
|
XP_011522131.1:n.1746+1G>A
|
|
|
XM_011523830.1:c.1725+1G>A
|
XP_011522132.1:n.1725+1G>A
|
|
|
XR_934021.1:n.1930+1G>A
|
|
|
|
XR_934022.1:n.1836+1G>A
|
|
|
|
XR_934023.1:n.1857+1G>A
|
|
|
|
XM_006721516.3:c.1848+1G>A
|
XP_006721579.2:n.1848+1G>A
|
|
|
XM_011523829.2:c.1746+1G>A
|
XP_011522131.1:n.1746+1G>A
|
|
|
XM_011523830.2:c.1725+1G>A
|
XP_011522132.1:n.1725+1G>A
|
|
|
XM_024450741.1:c.1815+1G>A
|
XP_024306509.1:n.1815+1G>A
|
|
|
XR_934021.2:n.1882+1G>A
|
|
|
|
XR_934022.2:n.1788+1G>A
|
|
|
|
XR_934023.2:n.1809+1G>A
|
|
|
|
NM_000018.4:c.1827+1G>A
MANE Select
|
NP_000009.1:n.1827+1G>A
|
|
|
NM_001033859.3:c.1761+1G>A
|
NP_001029031.1:n.1761+1G>A
|
|
|
NM_001270447.2:c.1896+1G>A
|
NP_001257376.1:n.1896+1G>A
|
|
|
NM_001270448.2:c.1599+1G>A
|
NP_001257377.1:n.1599+1G>A
|
|
