ENST00000681320.1:c.7484C>G
MANE Select
|
ENSP00000506558.1:p.Thr2495Arg
|
|
ENST00000328333.12:c.7484C>G
|
ENSP00000332371.8:p.Thr2495Arg
|
|
ENST00000422991.1:c.479C>G
|
ENSP00000391608.1:p.Thr160Arg
|
|
ENST00000459756.5:n.307C>G
|
|
|
ENST00000467985.1:n.330C>G
|
|
|
ENST00000487017.5:n.4123C>G
|
|
|
NM_000094.3:c.7484C>G , LRG_286t1:c.7484C>G
|
NP_000085.1:p.Thr2495Arg
|
|
XM_011533336.1:c.7511C>G
|
XP_011531638.1:p.Thr2504Arg
|
|
XM_011533337.1:c.7484C>G
|
XP_011531639.1:p.Thr2495Arg
|
|
XM_011533338.1:c.7451C>G
|
XP_011531640.1:p.Thr2484Arg
|
|
XM_011533339.1:c.7511C>G
|
XP_011531641.1:p.Thr2504Arg
|
|
XM_011533342.1:c.*39C>G
|
XP_011531644.1:n.*39C>G
|
|
XR_940369.1:n.7547C>G
|
|
|
XR_940370.1:n.7547C>G
|
|
|
XR_940371.1:n.7547C>G
|
|
|
XR_940372.1:n.7521C>G
|
|
|
XM_017005688.1:c.7424C>G
|
XP_016861177.1:p.Thr2475Arg
|
|
XM_017005689.1:c.7484C>G
|
XP_016861178.1:p.Thr2495Arg
|
|
XM_017005692.1:c.*39C>G
|
XP_016861181.1:n.*39C>G
|
|
XR_001740003.1:n.7520C>G
|
|
|
XR_001740004.1:n.7520C>G
|
|
|
XR_001740005.1:n.7520C>G
|
|
|
XR_001740006.1:n.7494C>G
|
|
|
NM_000094.4:c.7484C>G
MANE Select
|
NP_000085.1:p.Thr2495Arg
|
|