ENST00000317961.9:c.*226G>A
MANE Select
|
ENSP00000322408.4:n.*226G>A
|
|
ENST00000317961.8:c.*226G>A
|
ENSP00000322408.4:n.*226G>A
|
|
ENST00000382806.6:c.*226G>A
|
ENSP00000372256.2:n.*226G>A
|
|
ENST00000469599.6:n.3597G>A
|
|
|
ENST00000492117.1:n.4891G>A
|
|
|
ENST00000541639.5:c.*226G>A
|
ENSP00000444293.1:n.*226G>A
|
|
NM_001146705.1:c.*226G>A
|
NP_001140177.1:n.*226G>A
|
|
NM_001146706.1:c.*226G>A
|
NP_001140178.1:n.*226G>A
|
|
NM_004653.4:c.*226G>A
|
NP_004644.2:n.*226G>A
|
|
XM_005262560.1:c.*226G>A
|
XP_005262617.1:n.*226G>A
|
|
XM_005262561.1:c.*226G>A
|
XP_005262618.1:n.*226G>A
|
|
XM_011531468.1:c.*226G>A
|
XP_011529770.1:n.*226G>A
|
|
XR_430568.2:n.5621G>A
|
|
|
XM_005262560.3:c.*226G>A
|
XP_005262617.1:n.*226G>A
|
|
XM_005262561.3:c.*226G>A
|
XP_005262618.1:n.*226G>A
|
|
XM_011531468.3:c.*226G>A
|
XP_011529770.1:n.*226G>A
|
|
XM_024452495.1:c.*226G>A
|
XP_024308263.1:n.*226G>A
|
|
XM_024452496.1:c.*226G>A
|
XP_024308264.1:n.*226G>A
|
|
XR_001756009.2:n.5584G>A
|
|
|
XR_001756010.2:n.5552G>A
|
|
|
XR_001756011.2:n.5449G>A
|
|
|
XR_001756012.2:n.5597G>A
|
|
|
XR_001756013.2:n.4915G>A
|
|
|
XR_002958832.1:n.5169G>A
|
|
|
XR_002958834.1:n.5240G>A
|
|
|
XR_002958835.1:n.5123G>A
|
|
|
XR_002958836.1:n.5774G>A
|
|
|
XR_002958837.1:n.5581G>A
|
|
|
XR_244571.4:n.5101G>A
|
|
|
XR_430568.4:n.5620G>A
|
|
|
NM_001146706.2:c.*226G>A
|
NP_001140178.1:n.*226G>A
|
|
NM_004653.5:c.*226G>A
MANE Select
|
NP_004644.2:n.*226G>A
|
|
NM_001146705.2:c.*226G>A
|
NP_001140177.1:n.*226G>A
|
|