ENST00000496887.7:c.619G=
|
ENSP00000434560.2:p.Val207=
|
|
ENST00000646564.2:c.478-10490G=
|
ENSP00000495806.2:n.478-10490G=
|
|
ENST00000155840.12:c.880G=
MANE Select
|
ENSP00000155840.2:p.Val294=
|
|
ENST00000335475.6:c.499G=
|
ENSP00000334497.5:p.Val167=
|
|
ENST00000646564.1:c.124-10490G=
|
ENSP00000495806.1:n.124-10490G=
|
|
ENST00000155840.9:c.880G=
|
ENSP00000155840.2:p.Val294=
|
|
ENST00000335475.5:c.499G=
|
ENSP00000334497.5:p.Val167=
|
|
NM_000218.2:c.880G= , LRG_287t1:c.880G=
|
NP_000209.2:p.Val294=
|
|
NM_181798.1:c.499G= , LRG_287t2:c.499G=
|
NP_861463.1:p.Val167=
|
|
NM_000218.3:c.880G=
MANE Select
|
NP_000209.2:p.Val294=
|
|