ENST00000681320.1:c.7398G>T
MANE Select
|
ENSP00000506558.1:p.Gly2466=
|
|
ENST00000328333.12:c.7398G>T
|
ENSP00000332371.8:p.Gly2466=
|
|
ENST00000422991.1:c.393G>T
|
ENSP00000391608.1:p.Gly131=
|
|
ENST00000459756.5:n.125G>T
|
|
|
ENST00000467985.1:n.148G>T
|
|
|
ENST00000487017.5:n.4037G>T
|
|
|
NM_000094.3:c.7398G>T , LRG_286t1:c.7398G>T
|
NP_000085.1:p.Gly2466=
|
|
XM_011533336.1:c.7425G>T
|
XP_011531638.1:p.Gly2475=
|
|
XM_011533337.1:c.7398G>T
|
XP_011531639.1:p.Gly2466=
|
|
XM_011533338.1:c.7408-139G>T
|
XP_011531640.1:n.7408-139G>T
|
|
XM_011533339.1:c.7425G>T
|
XP_011531641.1:p.Gly2475=
|
|
XM_011533340.1:c.7408-65G>T
|
XP_011531642.1:n.7408-65G>T
|
|
XM_011533341.1:c.7382-65G>T
|
XP_011531643.1:n.7382-65G>T
|
|
XM_011533342.1:c.7382-139G>T
|
XP_011531644.1:n.7382-139G>T
|
|
XR_940369.1:n.7461G>T
|
|
|
XR_940370.1:n.7461G>T
|
|
|
XR_940371.1:n.7461G>T
|
|
|
XR_940372.1:n.7435G>T
|
|
|
XM_017005688.1:c.7381-139G>T
|
XP_016861177.1:n.7381-139G>T
|
|
XM_017005689.1:c.7398G>T
|
XP_016861178.1:p.Gly2466=
|
|
XM_017005690.1:c.7381-65G>T
|
XP_016861179.1:n.7381-65G>T
|
|
XM_017005691.1:c.7355-65G>T
|
XP_016861180.1:n.7355-65G>T
|
|
XM_017005692.1:c.7355-139G>T
|
XP_016861181.1:n.7355-139G>T
|
|
XR_001740003.1:n.7434G>T
|
|
|
XR_001740004.1:n.7434G>T
|
|
|
XR_001740005.1:n.7434G>T
|
|
|
XR_001740006.1:n.7408G>T
|
|
|
NM_000094.4:c.7398G>T
MANE Select
|
NP_000085.1:p.Gly2466=
|
|