ENST00000317961.9:c.971A>T
MANE Select
|
ENSP00000322408.4:p.Asp324Val
|
|
ENST00000317961.8:c.971A>T
|
ENSP00000322408.4:p.Asp324Val
|
|
ENST00000382806.6:c.800A>T
|
ENSP00000372256.2:p.Asp267Val
|
|
ENST00000440077.5:c.848A>T
|
ENSP00000398543.1:p.Asp283Val
|
|
ENST00000447300.1:c.836A>T
|
ENSP00000416377.1:p.Asp279Val
|
|
ENST00000541639.5:c.971A>T
|
ENSP00000444293.1:p.Asp324Val
|
|
NM_001146705.1:c.971A>T
|
NP_001140177.1:p.Asp324Val
|
|
NM_001146706.1:c.800A>T
|
NP_001140178.1:p.Asp267Val
|
|
NM_004653.4:c.971A>T
|
NP_004644.2:p.Asp324Val
|
|
XM_005262560.1:c.836A>T
|
XP_005262617.1:p.Asp279Val
|
|
XM_005262561.1:c.971A>T
|
XP_005262618.1:p.Asp324Val
|
|
XM_005262562.2:c.971A>T
|
XP_005262619.1:p.Asp324Val
|
|
XM_011531468.1:c.971A>T
|
XP_011529770.1:p.Asp324Val
|
|
XR_244571.2:n.1259A>T
|
|
|
XR_430568.2:n.1259A>T
|
|
|
XR_938609.1:n.1259A>T
|
|
|
XR_938610.1:n.1259A>T
|
|
|
XM_005262560.3:c.836A>T
|
XP_005262617.1:p.Asp279Val
|
|
XM_005262561.3:c.971A>T
|
XP_005262618.1:p.Asp324Val
|
|
XM_011531468.3:c.971A>T
|
XP_011529770.1:p.Asp324Val
|
|
XM_024452495.1:c.-1147A>T
|
XP_024308263.1:n.-1147A>T
|
|
XR_001756009.2:n.1258A>T
|
|
|
XR_001756010.2:n.1258A>T
|
|
|
XR_001756011.2:n.1123A>T
|
|
|
XR_001756012.2:n.1258A>T
|
|
|
XR_001756013.2:n.1258A>T
|
|
|
XR_002958832.1:n.1258A>T
|
|
|
XR_002958833.1:n.1258A>T
|
|
|
XR_002958834.1:n.1258A>T
|
|
|
XR_002958835.1:n.1258A>T
|
|
|
XR_002958836.1:n.1258A>T
|
|
|
XR_002958837.1:n.1258A>T
|
|
|
XR_244571.4:n.1258A>T
|
|
|
XR_430568.4:n.1258A>T
|
|
|
NM_001146706.2:c.800A>T
|
NP_001140178.1:p.Asp267Val
|
|
NM_004653.5:c.971A>T
MANE Select
|
NP_004644.2:p.Asp324Val
|
|
NM_001146705.2:c.971A>T
|
NP_001140177.1:p.Asp324Val
|
|