ENST00000222399.11:c.4457C>G
(LAMB1)
MANE Select
|
ENSP00000222399.6:p.Thr1486Arg
|
|
ENST00000393561.6:c.4046C>G
(LAMB1)
|
ENSP00000377191.2:p.Thr1349Arg
|
|
ENST00000468518.2:n.2691C>G
(LAMB1)
|
|
|
ENST00000468999.2:n.2605C>G
(LAMB1)
|
|
|
ENST00000474380.2:n.1272C>G
(LAMB1)
|
|
|
ENST00000676574.1:c.*373C>G
(LAMB1)
|
ENSP00000503081.1:n.*373C>G
|
|
ENST00000676744.1:n.303C>G
(LAMB1)
|
|
|
ENST00000676777.1:c.4457C>G
(LAMB1)
|
ENSP00000504756.1:p.Thr1486Arg
|
|
ENST00000677101.1:c.*4093C>G
(LAMB1)
|
ENSP00000503156.1:n.*4093C>G
|
|
ENST00000677144.1:c.*1276C>G
(LAMB1)
|
ENSP00000503049.1:n.*1276C>G
|
|
ENST00000677485.1:n.5681C>G
(LAMB1)
|
|
|
ENST00000677588.1:c.*688C>G
(LAMB1)
|
ENSP00000502938.1:n.*688C>G
|
|
ENST00000677793.1:c.4145C>G
(LAMB1)
|
ENSP00000504020.1:p.Thr1382Arg
|
|
ENST00000677801.1:c.*286C>G
(LAMB1)
|
ENSP00000503438.1:n.*286C>G
|
|
ENST00000678232.1:n.4646C>G
(LAMB1)
|
|
|
ENST00000678310.1:n.2626C>G
(LAMB1)
|
|
|
ENST00000678698.1:c.*529C>G
(LAMB1)
|
ENSP00000503198.1:n.*529C>G
|
|
ENST00000678704.1:c.*3039C>G
(LAMB1)
|
ENSP00000504589.1:n.*3039C>G
|
|
ENST00000678892.1:c.*529C>G
(LAMB1)
|
ENSP00000504841.1:n.*529C>G
|
|
ENST00000679200.1:c.*529C>G
(LAMB1)
|
ENSP00000503498.1:n.*529C>G
|
|
ENST00000222399.10:c.4457C>G
(LAMB1)
|
ENSP00000222399.6:p.Thr1486Arg
|
|
ENST00000393561.5:c.4529C>G
(LAMB1)
|
ENSP00000377191.1:p.Thr1510Arg
|
|
ENST00000417551.5:c.*130G>C
(DLD)
|
ENSP00000390667.1:n.*130G>C
|
|
ENST00000468518.1:n.516C>G
(LAMB1)
|
|
|
ENST00000474380.1:n.694C>G
(LAMB1)
|
|
|
NM_002291.2:c.4457C>G
(LAMB1)
|
NP_002282.2:p.Thr1486Arg
|
|
XM_017012201.1:c.4529C>G
(LAMB1)
|
XP_016867690.1:p.Thr1510Arg
|
|
XR_001744756.1:n.5376C>G
(LAMB1)
|
|
|
NM_002291.3:c.4457C>G
(LAMB1)
MANE Select
|
NP_002282.2:p.Thr1486Arg
|
|