ENST00000681320.1:c.7747C>G
MANE Select
|
ENSP00000506558.1:p.Leu2583Val
|
|
ENST00000328333.12:c.7747C>G
|
ENSP00000332371.8:p.Leu2583Val
|
|
ENST00000459756.5:n.570C>G
|
|
|
ENST00000467985.1:n.593C>G
|
|
|
ENST00000487017.5:n.4386C>G
|
|
|
NM_000094.3:c.7747C>G , LRG_286t1:c.7747C>G
|
NP_000085.1:p.Leu2583Val
|
|
XM_011533336.1:c.7774C>G
|
XP_011531638.1:p.Leu2592Val
|
|
XM_011533337.1:c.7747C>G
|
XP_011531639.1:p.Leu2583Val
|
|
XM_011533338.1:c.7714C>G
|
XP_011531640.1:p.Leu2572Val
|
|
XM_011533339.1:c.7774C>G
|
XP_011531641.1:p.Leu2592Val
|
|
XR_940369.1:n.7810C>G
|
|
|
XR_940370.1:n.7810C>G
|
|
|
XR_940371.1:n.7810C>G
|
|
|
XR_940372.1:n.7784C>G
|
|
|
XM_017005688.1:c.7687C>G
|
XP_016861177.1:p.Leu2563Val
|
|
XM_017005689.1:c.7747C>G
|
XP_016861178.1:p.Leu2583Val
|
|
XR_001740003.1:n.7783C>G
|
|
|
XR_001740004.1:n.7783C>G
|
|
|
XR_001740005.1:n.7783C>G
|
|
|
XR_001740006.1:n.7757C>G
|
|
|
NM_000094.4:c.7747C>G
MANE Select
|
NP_000085.1:p.Leu2583Val
|
|