ENST00000681320.1:c.7830A>G
MANE Select
|
ENSP00000506558.1:p.Arg2610=
|
|
ENST00000328333.12:c.7830A>G
|
ENSP00000332371.8:p.Arg2610=
|
|
ENST00000459756.5:n.653A>G
|
|
|
ENST00000487017.5:n.4469A>G
|
|
|
NM_000094.3:c.7830A>G , LRG_286t1:c.7830A>G
|
NP_000085.1:p.Arg2610=
|
|
XM_011533336.1:c.7857A>G
|
XP_011531638.1:p.Arg2619=
|
|
XM_011533337.1:c.7830A>G
|
XP_011531639.1:p.Arg2610=
|
|
XM_011533338.1:c.7797A>G
|
XP_011531640.1:p.Arg2599=
|
|
XR_940369.1:n.7893A>G
|
|
|
XR_940370.1:n.7893A>G
|
|
|
XR_940371.1:n.7893A>G
|
|
|
XR_940372.1:n.7867A>G
|
|
|
XM_017005688.1:c.7770A>G
|
XP_016861177.1:p.Arg2590=
|
|
XR_001740003.1:n.7866A>G
|
|
|
XR_001740004.1:n.7866A>G
|
|
|
XR_001740005.1:n.7866A>G
|
|
|
XR_001740006.1:n.7840A>G
|
|
|
NM_000094.4:c.7830A>G
MANE Select
|
NP_000085.1:p.Arg2610=
|
|