ENST00000496887.7:c.523C>T
|
ENSP00000434560.2:p.Leu175=
|
|
ENST00000646564.2:c.478-10586C>T
|
ENSP00000495806.2:n.478-10586C>T
|
|
ENST00000155840.12:c.784C>T
MANE Select
|
ENSP00000155840.2:p.Leu262=
|
|
ENST00000335475.6:c.403C>T
|
ENSP00000334497.5:p.Leu135=
|
|
ENST00000646564.1:c.124-10586C>T
|
ENSP00000495806.1:n.124-10586C>T
|
|
ENST00000155840.9:c.784C>T
|
ENSP00000155840.2:p.Leu262=
|
|
ENST00000335475.5:c.403C>T
|
ENSP00000334497.5:p.Leu135=
|
|
ENST00000496887.6:c.523C>T
|
ENSP00000434560.1:p.Leu175=
|
|
NM_000218.2:c.784C>T , LRG_287t1:c.784C>T
|
NP_000209.2:p.Leu262=
|
|
NM_181798.1:c.403C>T , LRG_287t2:c.403C>T
|
NP_861463.1:p.Leu135=
|
|
NM_000218.3:c.784C>T
MANE Select
|
NP_000209.2:p.Leu262=
|
|