|
ENST00000222399.11:c.4495G>C
(LAMB1)
MANE Select
|
ENSP00000222399.6:p.Glu1499Gln
|
|
|
ENST00000393561.6:c.4084G>C
(LAMB1)
|
ENSP00000377191.2:p.Glu1362Gln
|
|
|
ENST00000468518.2:n.2729G>C
(LAMB1)
|
|
|
|
ENST00000468999.2:n.2643G>C
(LAMB1)
|
|
|
|
ENST00000474380.2:n.1310G>C
(LAMB1)
|
|
|
|
ENST00000676574.1:c.*411G>C
(LAMB1)
|
ENSP00000503081.1:n.*411G>C
|
|
|
ENST00000676744.1:n.341G>C
(LAMB1)
|
|
|
|
ENST00000676777.1:c.4495G>C
(LAMB1)
|
ENSP00000504756.1:p.Glu1499Gln
|
|
|
ENST00000677101.1:c.*4131G>C
(LAMB1)
|
ENSP00000503156.1:n.*4131G>C
|
|
|
ENST00000677144.1:c.*1314G>C
(LAMB1)
|
ENSP00000503049.1:n.*1314G>C
|
|
|
ENST00000677485.1:n.5719G>C
(LAMB1)
|
|
|
|
ENST00000677588.1:c.*726G>C
(LAMB1)
|
ENSP00000502938.1:n.*726G>C
|
|
|
ENST00000677793.1:c.4183G>C
(LAMB1)
|
ENSP00000504020.1:p.Glu1395Gln
|
|
|
ENST00000677801.1:c.*324G>C
(LAMB1)
|
ENSP00000503438.1:n.*324G>C
|
|
|
ENST00000677883.1:n.6G>C
(LAMB1)
|
|
|
|
ENST00000678232.1:n.4684G>C
(LAMB1)
|
|
|
|
ENST00000678310.1:n.2664G>C
(LAMB1)
|
|
|
|
ENST00000678698.1:c.*567G>C
(LAMB1)
|
ENSP00000503198.1:n.*567G>C
|
|
|
ENST00000678704.1:c.*3077G>C
(LAMB1)
|
ENSP00000504589.1:n.*3077G>C
|
|
|
ENST00000678892.1:c.*567G>C
(LAMB1)
|
ENSP00000504841.1:n.*567G>C
|
|
|
ENST00000679200.1:c.*567G>C
(LAMB1)
|
ENSP00000503498.1:n.*567G>C
|
|
|
ENST00000222399.10:c.4495G>C
(LAMB1)
|
ENSP00000222399.6:p.Glu1499Gln
|
|
|
ENST00000393561.5:c.4567G>C
(LAMB1)
|
ENSP00000377191.1:p.Glu1523Gln
|
|
|
ENST00000417551.5:c.*125-33C>G
(DLD)
|
ENSP00000390667.1:n.*125-33C>G
|
|
|
ENST00000468518.1:n.554G>C
(LAMB1)
|
|
|
|
ENST00000474380.1:n.732G>C
(LAMB1)
|
|
|
|
NM_002291.2:c.4495G>C
(LAMB1)
|
NP_002282.2:p.Glu1499Gln
|
|
|
XM_017012201.1:c.4567G>C
(LAMB1)
|
XP_016867690.1:p.Glu1523Gln
|
|
|
XR_001744756.1:n.5414G>C
(LAMB1)
|
|
|
|
NM_002291.3:c.4495G>C
(LAMB1)
MANE Select
|
NP_002282.2:p.Glu1499Gln
|
|
