ENST00000480266.6:c.672C>A
|
ENSP00000479015.1:p.Arg224=
|
|
ENST00000373203.9:c.1218C>A
MANE Select
|
ENSP00000362299.4:p.Arg406=
|
|
ENST00000344849.4:c.1218C>A
|
ENSP00000341917.3:p.Arg406=
|
|
ENST00000373203.8:c.1218C>A
|
ENSP00000362299.4:p.Arg406=
|
|
ENST00000480266.5:c.672C>A
|
ENSP00000479015.1:p.Arg224=
|
|
ENST00000486329.1:n.186C>A
|
|
|
NM_000118.3:c.1218C>A , LRG_589t1:c.1218C>A
|
NP_000109.1:p.Arg406=
|
|
NM_001114753.2:c.1218C>A , LRG_589t2:c.1218C>A
|
NP_001108225.1:p.Arg406=
|
|
NM_001278138.1:c.672C>A
|
NP_001265067.1:p.Arg224=
|
|
NR_136302.1:n.1569-1241G>T
|
|
|
NM_001114753.3:c.1218C>A
MANE Select
|
NP_001108225.1:p.Arg406=
|
|
NM_001278138.2:c.672C>A
|
NP_001265067.1:p.Arg224=
|
|