|
ENST00000222399.11:c.4433G>A
(LAMB1)
MANE Select
|
ENSP00000222399.6:p.Ser1478Asn
|
|
|
ENST00000393561.6:c.4022G>A
(LAMB1)
|
ENSP00000377191.2:p.Ser1341Asn
|
|
|
ENST00000468518.2:n.2667G>A
(LAMB1)
|
|
|
|
ENST00000468999.2:n.2581G>A
(LAMB1)
|
|
|
|
ENST00000474380.2:n.1248G>A
(LAMB1)
|
|
|
|
ENST00000676574.1:c.*349G>A
(LAMB1)
|
ENSP00000503081.1:n.*349G>A
|
|
|
ENST00000676744.1:n.279G>A
(LAMB1)
|
|
|
|
ENST00000676777.1:c.4433G>A
(LAMB1)
|
ENSP00000504756.1:p.Ser1478Asn
|
|
|
ENST00000677101.1:c.*4069G>A
(LAMB1)
|
ENSP00000503156.1:n.*4069G>A
|
|
|
ENST00000677144.1:c.*1252G>A
(LAMB1)
|
ENSP00000503049.1:n.*1252G>A
|
|
|
ENST00000677485.1:n.5657G>A
(LAMB1)
|
|
|
|
ENST00000677588.1:c.*664G>A
(LAMB1)
|
ENSP00000502938.1:n.*664G>A
|
|
|
ENST00000677793.1:c.4121G>A
(LAMB1)
|
ENSP00000504020.1:p.Ser1374Asn
|
|
|
ENST00000677801.1:c.*262G>A
(LAMB1)
|
ENSP00000503438.1:n.*262G>A
|
|
|
ENST00000678232.1:n.4622G>A
(LAMB1)
|
|
|
|
ENST00000678310.1:n.2602G>A
(LAMB1)
|
|
|
|
ENST00000678698.1:c.*505G>A
(LAMB1)
|
ENSP00000503198.1:n.*505G>A
|
|
|
ENST00000678704.1:c.*3015G>A
(LAMB1)
|
ENSP00000504589.1:n.*3015G>A
|
|
|
ENST00000678892.1:c.*505G>A
(LAMB1)
|
ENSP00000504841.1:n.*505G>A
|
|
|
ENST00000679200.1:c.*505G>A
(LAMB1)
|
ENSP00000503498.1:n.*505G>A
|
|
|
ENST00000222399.10:c.4433G>A
(LAMB1)
|
ENSP00000222399.6:p.Ser1478Asn
|
|
|
ENST00000393561.5:c.4505G>A
(LAMB1)
|
ENSP00000377191.1:p.Ser1502Asn
|
|
|
ENST00000417551.5:c.*154C>T
(DLD)
|
ENSP00000390667.1:n.*154C>T
|
|
|
ENST00000468518.1:n.492G>A
(LAMB1)
|
|
|
|
ENST00000474380.1:n.670G>A
(LAMB1)
|
|
|
|
NM_002291.2:c.4433G>A
(LAMB1)
|
NP_002282.2:p.Ser1478Asn
|
|
|
XM_017012201.1:c.4505G>A
(LAMB1)
|
XP_016867690.1:p.Ser1502Asn
|
|
|
XR_001744756.1:n.5352G>A
(LAMB1)
|
|
|
|
NM_002291.3:c.4433G>A
(LAMB1)
MANE Select
|
NP_002282.2:p.Ser1478Asn
|
|
