|
ENST00000538183.7:c.249T>G
MANE Select
|
ENSP00000446252.1:p.Ala83=
|
|
|
ENST00000337404.8:c.227-3187T>G
|
ENSP00000337127.4:n.227-3187T>G
|
|
|
ENST00000367054.6:c.227-3187T>G
|
ENSP00000356021.2:n.227-3187T>G
|
|
|
ENST00000367055.8:c.249T>G
|
ENSP00000356022.4:p.Ala83=
|
|
|
ENST00000401980.3:c.89-3187T>G
|
ENSP00000384196.3:n.89-3187T>G
|
|
|
ENST00000444946.6:c.249T>G
|
ENSP00000404804.2:p.Ala83=
|
|
|
ENST00000535459.5:n.129T>G
|
|
|
|
ENST00000535561.5:c.318T>G
|
ENSP00000445015.1:p.Ala106=
|
|
|
ENST00000537657.5:c.111T>G
|
ENSP00000439191.1:p.Ala37=
|
|
|
ENST00000538183.6:c.249T>G
|
ENSP00000446252.1:p.Ala83=
|
|
|
ENST00000540491.1:n.246-3187T>G
|
|
|
|
ENST00000541573.5:n.142T>G
|
|
|
|
ENST00000545162.5:c.318T>G
|
ENSP00000441362.1:p.Ala106=
|
|
|
ENST00000546087.5:c.111T>G
|
ENSP00000442920.1:p.Ala37=
|
|
|
ENST00000546260.5:c.379T>G
|
ENSP00000440131.1:p.Ser127Ala
|
|
|
NM_000636.2:c.249T>G
|
NP_000627.2:p.Ala83=
|
|
|
NM_001024465.1:c.249T>G
|
NP_001019636.1:p.Ala83=
|
|
|
NM_001024466.1:c.227-3187T>G
|
NP_001019637.1:n.227-3187T>G
|
|
|
NM_000636.3:c.249T>G
|
NP_000627.2:p.Ala83=
|
|
|
NM_001024465.2:c.249T>G
|
NP_001019636.1:p.Ala83=
|
|
|
NM_001024466.2:c.227-3187T>G
|
NP_001019637.1:n.227-3187T>G
|
|
|
NM_001322814.1:c.227-3187T>G
|
NP_001309743.1:n.227-3187T>G
|
|
|
NM_001322815.1:c.249T>G
|
NP_001309744.1:p.Ala83=
|
|
|
NM_001322817.1:c.111T>G
|
NP_001309746.1:p.Ala37=
|
|
|
NM_001322819.1:c.111T>G
|
NP_001309748.1:p.Ala37=
|
|
|
NM_001322820.1:c.111T>G
|
NP_001309749.1:p.Ala37=
|
|
|
NM_000636.4:c.249T>G
MANE Select
|
NP_000627.2:p.Ala83=
|
|
|
NM_001024465.3:c.249T>G
|
NP_001019636.1:p.Ala83=
|
|
|
NM_001024466.3:c.227-3187T>G
|
NP_001019637.1:n.227-3187T>G
|
|
|
NM_001322814.2:c.227-3187T>G
|
NP_001309743.1:n.227-3187T>G
|
|
|
NM_001322815.2:c.249T>G
|
NP_001309744.1:p.Ala83=
|
|
|
NM_001322817.2:c.111T>G
|
NP_001309746.1:p.Ala37=
|
|
|
NM_001322819.2:c.111T>G
|
NP_001309748.1:p.Ala37=
|
|
|
NM_001322820.2:c.111T>G
|
NP_001309749.1:p.Ala37=
|
|
