ENST00000681320.1:c.8389G>A
MANE Select
|
ENSP00000506558.1:p.Glu2797Lys
|
|
ENST00000328333.12:c.8389G>A
|
ENSP00000332371.8:p.Glu2797Lys
|
|
ENST00000487017.5:n.5028G>A
|
|
|
NM_000094.3:c.8389G>A , LRG_286t1:c.8389G>A
|
NP_000085.1:p.Glu2797Lys
|
|
XM_011533336.1:c.8416G>A
|
XP_011531638.1:p.Glu2806Lys
|
|
XM_011533337.1:c.8389G>A
|
XP_011531639.1:p.Glu2797Lys
|
|
XM_011533338.1:c.8356G>A
|
XP_011531640.1:p.Glu2786Lys
|
|
XR_940369.1:n.8452G>A
|
|
|
XR_940370.1:n.8452G>A
|
|
|
XR_940371.1:n.8452G>A
|
|
|
XM_017005688.1:c.8329G>A
|
XP_016861177.1:p.Glu2777Lys
|
|
XR_001740003.1:n.8425G>A
|
|
|
XR_001740004.1:n.8425G>A
|
|
|
XR_001740005.1:n.8425G>A
|
|
|
NM_000094.4:c.8389G>A
MANE Select
|
NP_000085.1:p.Glu2797Lys
|
|