ENST00000287957.5:c.309T=
MANE Select
|
ENSP00000287957.3:p.Ala103=
|
|
ENST00000644160.1:n.165T=
|
|
|
ENST00000645746.1:c.309T=
|
ENSP00000493785.1:p.Ala103=
|
|
ENST00000287957.3:c.309T=
|
ENSP00000287957.3:p.Ala103=
|
|
NM_021167.4:c.309T=
|
NP_066990.3:p.Ala103=
|
|
NR_052016.1:n.591T=
|
|
|
XR_428182.2:n.564T=
|
|
|
XR_927494.1:n.564T=
|
|
|
XR_927495.1:n.564T=
|
|
|
XR_927496.1:n.564T=
|
|
|
XR_927497.1:n.564T=
|
|
|
XR_927498.1:n.564T=
|
|
|
XR_927499.1:n.564T=
|
|
|
XR_927500.1:n.564T=
|
|
|
XR_927501.1:n.564T=
|
|
|
XR_927502.1:n.564T=
|
|
|
XR_927503.1:n.564T=
|
|
|
XR_927504.1:n.564T=
|
|
|
XR_001744842.2:n.591T=
|
|
|
XR_001744843.2:n.591T=
|
|
|
XR_002956472.1:n.591T=
|
|
|
XR_002956473.1:n.591T=
|
|
|
XR_002956474.1:n.591T=
|
|
|
XR_002956475.1:n.557T=
|
|
|
XR_002956476.1:n.557T=
|
|
|
XR_927494.3:n.591T=
|
|
|
XR_927500.3:n.591T=
|
|
|
XR_927503.3:n.591T=
|
|
|
NM_021167.5:c.309T=
MANE Select
|
NP_066990.3:p.Ala103=
|
|
NR_052016.2:n.557T=
|
|
|