ENST00000496887.7:c.447G>T
|
ENSP00000434560.2:p.Leu149=
|
|
ENST00000646564.2:c.478-11398G>T
|
ENSP00000495806.2:n.478-11398G>T
|
|
ENST00000155840.12:c.708G>T
MANE Select
|
ENSP00000155840.2:p.Leu236=
|
|
ENST00000335475.6:c.327G>T
|
ENSP00000334497.5:p.Leu109=
|
|
ENST00000646564.1:c.124-11398G>T
|
ENSP00000495806.1:n.124-11398G>T
|
|
ENST00000155840.9:c.708G>T
|
ENSP00000155840.2:p.Leu236=
|
|
ENST00000335475.5:c.327G>T
|
ENSP00000334497.5:p.Leu109=
|
|
ENST00000496887.6:c.447G>T
|
ENSP00000434560.1:p.Leu149=
|
|
NM_000218.2:c.708G>T , LRG_287t1:c.708G>T
|
NP_000209.2:p.Leu236=
|
|
NM_181798.1:c.327G>T , LRG_287t2:c.327G>T
|
NP_861463.1:p.Leu109=
|
|
NM_000218.3:c.708G>T
MANE Select
|
NP_000209.2:p.Leu236=
|
|