|
ENST00000222399.11:c.4440A>C
(LAMB1)
MANE Select
|
ENSP00000222399.6:p.Glu1480Asp
|
|
|
ENST00000393561.6:c.4029A>C
(LAMB1)
|
ENSP00000377191.2:p.Glu1343Asp
|
|
|
ENST00000468518.2:n.2674A>C
(LAMB1)
|
|
|
|
ENST00000468999.2:n.2588A>C
(LAMB1)
|
|
|
|
ENST00000474380.2:n.1255A>C
(LAMB1)
|
|
|
|
ENST00000676574.1:c.*356A>C
(LAMB1)
|
ENSP00000503081.1:n.*356A>C
|
|
|
ENST00000676744.1:n.286A>C
(LAMB1)
|
|
|
|
ENST00000676777.1:c.4440A>C
(LAMB1)
|
ENSP00000504756.1:p.Glu1480Asp
|
|
|
ENST00000677101.1:c.*4076A>C
(LAMB1)
|
ENSP00000503156.1:n.*4076A>C
|
|
|
ENST00000677144.1:c.*1259A>C
(LAMB1)
|
ENSP00000503049.1:n.*1259A>C
|
|
|
ENST00000677485.1:n.5664A>C
(LAMB1)
|
|
|
|
ENST00000677588.1:c.*671A>C
(LAMB1)
|
ENSP00000502938.1:n.*671A>C
|
|
|
ENST00000677793.1:c.4128A>C
(LAMB1)
|
ENSP00000504020.1:p.Glu1376Asp
|
|
|
ENST00000677801.1:c.*269A>C
(LAMB1)
|
ENSP00000503438.1:n.*269A>C
|
|
|
ENST00000678232.1:n.4629A>C
(LAMB1)
|
|
|
|
ENST00000678310.1:n.2609A>C
(LAMB1)
|
|
|
|
ENST00000678698.1:c.*512A>C
(LAMB1)
|
ENSP00000503198.1:n.*512A>C
|
|
|
ENST00000678704.1:c.*3022A>C
(LAMB1)
|
ENSP00000504589.1:n.*3022A>C
|
|
|
ENST00000678892.1:c.*512A>C
(LAMB1)
|
ENSP00000504841.1:n.*512A>C
|
|
|
ENST00000679200.1:c.*512A>C
(LAMB1)
|
ENSP00000503498.1:n.*512A>C
|
|
|
ENST00000222399.10:c.4440A>C
(LAMB1)
|
ENSP00000222399.6:p.Glu1480Asp
|
|
|
ENST00000393561.5:c.4512A>C
(LAMB1)
|
ENSP00000377191.1:p.Glu1504Asp
|
|
|
ENST00000417551.5:c.*147T>G
(DLD)
|
ENSP00000390667.1:n.*147T>G
|
|
|
ENST00000468518.1:n.499A>C
(LAMB1)
|
|
|
|
ENST00000474380.1:n.677A>C
(LAMB1)
|
|
|
|
NM_002291.2:c.4440A>C
(LAMB1)
|
NP_002282.2:p.Glu1480Asp
|
|
|
XM_017012201.1:c.4512A>C
(LAMB1)
|
XP_016867690.1:p.Glu1504Asp
|
|
|
XR_001744756.1:n.5359A>C
(LAMB1)
|
|
|
|
NM_002291.3:c.4440A>C
(LAMB1)
MANE Select
|
NP_002282.2:p.Glu1480Asp
|
|
