|
ENST00000222399.11:c.4493A>C
(LAMB1)
MANE Select
|
ENSP00000222399.6:p.Glu1498Ala
|
|
|
ENST00000393561.6:c.4082A>C
(LAMB1)
|
ENSP00000377191.2:p.Glu1361Ala
|
|
|
ENST00000468518.2:n.2727A>C
(LAMB1)
|
|
|
|
ENST00000468999.2:n.2641A>C
(LAMB1)
|
|
|
|
ENST00000474380.2:n.1308A>C
(LAMB1)
|
|
|
|
ENST00000676574.1:c.*409A>C
(LAMB1)
|
ENSP00000503081.1:n.*409A>C
|
|
|
ENST00000676744.1:n.339A>C
(LAMB1)
|
|
|
|
ENST00000676777.1:c.4493A>C
(LAMB1)
|
ENSP00000504756.1:p.Glu1498Ala
|
|
|
ENST00000677101.1:c.*4129A>C
(LAMB1)
|
ENSP00000503156.1:n.*4129A>C
|
|
|
ENST00000677144.1:c.*1312A>C
(LAMB1)
|
ENSP00000503049.1:n.*1312A>C
|
|
|
ENST00000677485.1:n.5717A>C
(LAMB1)
|
|
|
|
ENST00000677588.1:c.*724A>C
(LAMB1)
|
ENSP00000502938.1:n.*724A>C
|
|
|
ENST00000677793.1:c.4181A>C
(LAMB1)
|
ENSP00000504020.1:p.Glu1394Ala
|
|
|
ENST00000677801.1:c.*322A>C
(LAMB1)
|
ENSP00000503438.1:n.*322A>C
|
|
|
ENST00000677883.1:n.4A>C
(LAMB1)
|
|
|
|
ENST00000678232.1:n.4682A>C
(LAMB1)
|
|
|
|
ENST00000678310.1:n.2662A>C
(LAMB1)
|
|
|
|
ENST00000678698.1:c.*565A>C
(LAMB1)
|
ENSP00000503198.1:n.*565A>C
|
|
|
ENST00000678704.1:c.*3075A>C
(LAMB1)
|
ENSP00000504589.1:n.*3075A>C
|
|
|
ENST00000678892.1:c.*565A>C
(LAMB1)
|
ENSP00000504841.1:n.*565A>C
|
|
|
ENST00000679200.1:c.*565A>C
(LAMB1)
|
ENSP00000503498.1:n.*565A>C
|
|
|
ENST00000222399.10:c.4493A>C
(LAMB1)
|
ENSP00000222399.6:p.Glu1498Ala
|
|
|
ENST00000393561.5:c.4565A>C
(LAMB1)
|
ENSP00000377191.1:p.Glu1522Ala
|
|
|
ENST00000417551.5:c.*125-31T>G
(DLD)
|
ENSP00000390667.1:n.*125-31T>G
|
|
|
ENST00000468518.1:n.552A>C
(LAMB1)
|
|
|
|
ENST00000474380.1:n.730A>C
(LAMB1)
|
|
|
|
NM_002291.2:c.4493A>C
(LAMB1)
|
NP_002282.2:p.Glu1498Ala
|
|
|
XM_017012201.1:c.4565A>C
(LAMB1)
|
XP_016867690.1:p.Glu1522Ala
|
|
|
XR_001744756.1:n.5412A>C
(LAMB1)
|
|
|
|
NM_002291.3:c.4493A>C
(LAMB1)
MANE Select
|
NP_002282.2:p.Glu1498Ala
|
|
