ENST00000480266.6:c.888A=
|
ENSP00000479015.1:p.Arg296=
|
|
ENST00000373203.9:c.1434A=
MANE Select
|
ENSP00000362299.4:p.Arg478=
|
|
ENST00000344849.4:c.1434A=
|
ENSP00000341917.3:p.Arg478=
|
|
ENST00000373203.8:c.1434A=
|
ENSP00000362299.4:p.Arg478=
|
|
ENST00000480266.5:c.888A=
|
ENSP00000479015.1:p.Arg296=
|
|
NM_000118.3:c.1434A= , LRG_589t1:c.1434A=
|
NP_000109.1:p.Arg478=
|
|
NM_001114753.2:c.1434A= , LRG_589t2:c.1434A=
|
NP_001108225.1:p.Arg478=
|
|
NM_001278138.1:c.888A=
|
NP_001265067.1:p.Arg296=
|
|
NR_136302.1:n.1439T=
|
|
|
NM_001114753.3:c.1434A=
MANE Select
|
NP_001108225.1:p.Arg478=
|
|
NM_001278138.2:c.888A=
|
NP_001265067.1:p.Arg296=
|
|