ENST00000681320.1:c.7809G>A
MANE Select
|
ENSP00000506558.1:p.Lys2603=
|
|
ENST00000328333.12:c.7809G>A
|
ENSP00000332371.8:p.Lys2603=
|
|
ENST00000459756.5:n.632G>A
|
|
|
ENST00000487017.5:n.4448G>A
|
|
|
NM_000094.3:c.7809G>A , LRG_286t1:c.7809G>A
|
NP_000085.1:p.Lys2603=
|
|
XM_011533336.1:c.7836G>A
|
XP_011531638.1:p.Lys2612=
|
|
XM_011533337.1:c.7809G>A
|
XP_011531639.1:p.Lys2603=
|
|
XM_011533338.1:c.7776G>A
|
XP_011531640.1:p.Lys2592=
|
|
XM_011533339.1:c.*41G>A
|
XP_011531641.1:n.*41G>A
|
|
XR_940369.1:n.7872G>A
|
|
|
XR_940370.1:n.7872G>A
|
|
|
XR_940371.1:n.7872G>A
|
|
|
XR_940372.1:n.7846G>A
|
|
|
XM_017005688.1:c.7749G>A
|
XP_016861177.1:p.Lys2583=
|
|
XM_017005689.1:c.*41G>A
|
XP_016861178.1:n.*41G>A
|
|
XR_001740003.1:n.7845G>A
|
|
|
XR_001740004.1:n.7845G>A
|
|
|
XR_001740005.1:n.7845G>A
|
|
|
XR_001740006.1:n.7819G>A
|
|
|
NM_000094.4:c.7809G>A
MANE Select
|
NP_000085.1:p.Lys2603=
|
|