|
ENST00000317961.9:c.933+1022G>T
MANE Select
|
ENSP00000322408.4:n.933+1022G>T
|
|
|
ENST00000317961.8:c.933+1022G>T
|
ENSP00000322408.4:n.933+1022G>T
|
|
|
ENST00000382806.6:c.762+1022G>T
|
ENSP00000372256.2:n.762+1022G>T
|
|
|
ENST00000440077.5:c.810+1022G>T
|
ENSP00000398543.1:n.810+1022G>T
|
|
|
ENST00000447300.1:c.798+1022G>T
|
ENSP00000416377.1:n.798+1022G>T
|
|
|
ENST00000541639.5:c.933+1022G>T
|
ENSP00000444293.1:n.933+1022G>T
|
|
|
NM_001146705.1:c.933+1022G>T
|
NP_001140177.1:n.933+1022G>T
|
|
|
NM_001146706.1:c.762+1022G>T
|
NP_001140178.1:n.762+1022G>T
|
|
|
NM_004653.4:c.933+1022G>T
|
NP_004644.2:n.933+1022G>T
|
|
|
XM_005262560.1:c.798+1022G>T
|
XP_005262617.1:n.798+1022G>T
|
|
|
XM_005262561.1:c.933+1022G>T
|
XP_005262618.1:n.933+1022G>T
|
|
|
XM_005262562.2:c.933+1022G>T
|
XP_005262619.1:n.933+1022G>T
|
|
|
XM_011531468.1:c.933+1022G>T
|
XP_011529770.1:n.933+1022G>T
|
|
|
XR_244571.2:n.1221+1022G>T
|
|
|
|
XR_430568.2:n.1221+1022G>T
|
|
|
|
XR_938609.1:n.1221+1022G>T
|
|
|
|
XR_938610.1:n.1221+1022G>T
|
|
|
|
XM_005262560.3:c.798+1022G>T
|
XP_005262617.1:n.798+1022G>T
|
|
|
XM_005262561.3:c.933+1022G>T
|
XP_005262618.1:n.933+1022G>T
|
|
|
XM_011531468.3:c.933+1022G>T
|
XP_011529770.1:n.933+1022G>T
|
|
|
XM_024452495.1:c.-1185+1022G>T
|
XP_024308263.1:n.-1185+1022G>T
|
|
|
XR_001756009.2:n.1220+1022G>T
|
|
|
|
XR_001756010.2:n.1220+1022G>T
|
|
|
|
XR_001756011.2:n.1085+1022G>T
|
|
|
|
XR_001756012.2:n.1220+1022G>T
|
|
|
|
XR_001756013.2:n.1220+1022G>T
|
|
|
|
XR_002958832.1:n.1220+1022G>T
|
|
|
|
XR_002958833.1:n.1220+1022G>T
|
|
|
|
XR_002958834.1:n.1220+1022G>T
|
|
|
|
XR_002958835.1:n.1220+1022G>T
|
|
|
|
XR_002958836.1:n.1220+1022G>T
|
|
|
|
XR_002958837.1:n.1220+1022G>T
|
|
|
|
XR_244571.4:n.1220+1022G>T
|
|
|
|
XR_430568.4:n.1220+1022G>T
|
|
|
|
NM_001146706.2:c.762+1022G>T
|
NP_001140178.1:n.762+1022G>T
|
|
|
NM_004653.5:c.933+1022G>T
MANE Select
|
NP_004644.2:n.933+1022G>T
|
|
|
NM_001146705.2:c.933+1022G>T
|
NP_001140177.1:n.933+1022G>T
|
|
