ENST00000681320.1:c.7427A>T
MANE Select
|
ENSP00000506558.1:p.Glu2476Val
|
|
ENST00000328333.12:c.7427A>T
|
ENSP00000332371.8:p.Glu2476Val
|
|
ENST00000422991.1:c.422A>T
|
ENSP00000391608.1:p.Glu141Val
|
|
ENST00000459756.5:n.154A>T
|
|
|
ENST00000467985.1:n.177A>T
|
|
|
ENST00000487017.5:n.4066A>T
|
|
|
NM_000094.3:c.7427A>T , LRG_286t1:c.7427A>T
|
NP_000085.1:p.Glu2476Val
|
|
XM_011533336.1:c.7454A>T
|
XP_011531638.1:p.Glu2485Val
|
|
XM_011533337.1:c.7427A>T
|
XP_011531639.1:p.Glu2476Val
|
|
XM_011533338.1:c.7408-110A>T
|
XP_011531640.1:n.7408-110A>T
|
|
XM_011533339.1:c.7454A>T
|
XP_011531641.1:p.Glu2485Val
|
|
XM_011533340.1:c.7408-36A>T
|
XP_011531642.1:n.7408-36A>T
|
|
XM_011533341.1:c.7382-36A>T
|
XP_011531643.1:n.7382-36A>T
|
|
XM_011533342.1:c.7382-110A>T
|
XP_011531644.1:n.7382-110A>T
|
|
XR_940369.1:n.7490A>T
|
|
|
XR_940370.1:n.7490A>T
|
|
|
XR_940371.1:n.7490A>T
|
|
|
XR_940372.1:n.7464A>T
|
|
|
XM_017005688.1:c.7381-110A>T
|
XP_016861177.1:n.7381-110A>T
|
|
XM_017005689.1:c.7427A>T
|
XP_016861178.1:p.Glu2476Val
|
|
XM_017005690.1:c.7381-36A>T
|
XP_016861179.1:n.7381-36A>T
|
|
XM_017005691.1:c.7355-36A>T
|
XP_016861180.1:n.7355-36A>T
|
|
XM_017005692.1:c.7355-110A>T
|
XP_016861181.1:n.7355-110A>T
|
|
XR_001740003.1:n.7463A>T
|
|
|
XR_001740004.1:n.7463A>T
|
|
|
XR_001740005.1:n.7463A>T
|
|
|
XR_001740006.1:n.7437A>T
|
|
|
NM_000094.4:c.7427A>T
MANE Select
|
NP_000085.1:p.Glu2476Val
|
|