|
ENST00000222399.11:c.4499T>G
(LAMB1)
MANE Select
|
ENSP00000222399.6:p.Leu1500Arg
|
|
|
ENST00000393561.6:c.4088T>G
(LAMB1)
|
ENSP00000377191.2:p.Leu1363Arg
|
|
|
ENST00000468518.2:n.2733T>G
(LAMB1)
|
|
|
|
ENST00000468999.2:n.2647T>G
(LAMB1)
|
|
|
|
ENST00000474380.2:n.1314T>G
(LAMB1)
|
|
|
|
ENST00000676574.1:c.*415T>G
(LAMB1)
|
ENSP00000503081.1:n.*415T>G
|
|
|
ENST00000676744.1:n.345T>G
(LAMB1)
|
|
|
|
ENST00000676777.1:c.4499T>G
(LAMB1)
|
ENSP00000504756.1:p.Leu1500Arg
|
|
|
ENST00000677101.1:c.*4135T>G
(LAMB1)
|
ENSP00000503156.1:n.*4135T>G
|
|
|
ENST00000677144.1:c.*1318T>G
(LAMB1)
|
ENSP00000503049.1:n.*1318T>G
|
|
|
ENST00000677485.1:n.5723T>G
(LAMB1)
|
|
|
|
ENST00000677588.1:c.*730T>G
(LAMB1)
|
ENSP00000502938.1:n.*730T>G
|
|
|
ENST00000677793.1:c.4187T>G
(LAMB1)
|
ENSP00000504020.1:p.Leu1396Arg
|
|
|
ENST00000677801.1:c.*328T>G
(LAMB1)
|
ENSP00000503438.1:n.*328T>G
|
|
|
ENST00000677883.1:n.10T>G
(LAMB1)
|
|
|
|
ENST00000678232.1:n.4688T>G
(LAMB1)
|
|
|
|
ENST00000678310.1:n.2668T>G
(LAMB1)
|
|
|
|
ENST00000678698.1:c.*571T>G
(LAMB1)
|
ENSP00000503198.1:n.*571T>G
|
|
|
ENST00000678704.1:c.*3081T>G
(LAMB1)
|
ENSP00000504589.1:n.*3081T>G
|
|
|
ENST00000678892.1:c.*571T>G
(LAMB1)
|
ENSP00000504841.1:n.*571T>G
|
|
|
ENST00000679200.1:c.*571T>G
(LAMB1)
|
ENSP00000503498.1:n.*571T>G
|
|
|
ENST00000222399.10:c.4499T>G
(LAMB1)
|
ENSP00000222399.6:p.Leu1500Arg
|
|
|
ENST00000393561.5:c.4571T>G
(LAMB1)
|
ENSP00000377191.1:p.Leu1524Arg
|
|
|
ENST00000417551.5:c.*125-37A>C
(DLD)
|
ENSP00000390667.1:n.*125-37A>C
|
|
|
ENST00000468518.1:n.558T>G
(LAMB1)
|
|
|
|
ENST00000474380.1:n.736T>G
(LAMB1)
|
|
|
|
NM_002291.2:c.4499T>G
(LAMB1)
|
NP_002282.2:p.Leu1500Arg
|
|
|
XM_017012201.1:c.4571T>G
(LAMB1)
|
XP_016867690.1:p.Leu1524Arg
|
|
|
XR_001744756.1:n.5418T>G
(LAMB1)
|
|
|
|
NM_002291.3:c.4499T>G
(LAMB1)
MANE Select
|
NP_002282.2:p.Leu1500Arg
|
|
