ENST00000700559.2:c.237A>G
|
ENSP00000515065.2:p.Arg79=
|
|
ENST00000700563.2:c.237A>G
|
ENSP00000515066.2:p.Arg79=
|
|
ENST00000700563.1:c.191A>G
|
|
|
ENST00000700564.1:n.241A>G
|
|
|
ENST00000700565.1:n.90A>G
|
|
|
ENST00000070846.11:c.237A>G
|
ENSP00000070846.6:p.Arg79=
|
|
ENST00000340811.9:c.237A>G
MANE Select
|
ENSP00000342800.5:p.Arg79=
|
|
ENST00000070846.10:c.237A>G
|
ENSP00000070846.6:p.Arg79=
|
|
ENST00000340811.8:c.237A>G
|
ENSP00000342800.4:p.Arg79=
|
|
ENST00000613243.1:c.237A>G
|
ENSP00000478295.1:p.Arg79=
|
|
NM_001005242.2:c.237A>G
|
NP_001005242.2:p.Arg79=
|
|
NM_004572.3:c.237A>G , LRG_398t1:c.237A>G
|
NP_004563.2:p.Arg79=
|
|
NM_001005242.3:c.237A>G
MANE Select
|
NP_001005242.2:p.Arg79=
|
|
NM_004572.4:c.237A>G
|
NP_004563.2:p.Arg79=
|
|