ENST00000340855.11:c.546G>T
MANE Select
|
ENSP00000339801.6:p.Leu182=
|
|
ENST00000651111.1:c.-88G>T
|
ENSP00000498395.1:n.-88G>T
|
|
ENST00000340855.10:c.546G>T
|
ENSP00000339801.6:p.Leu182=
|
|
ENST00000370441.8:c.546G>T
|
ENSP00000359470.4:p.Leu182=
|
|
ENST00000422081.6:c.-88G>T
|
ENSP00000477056.1:n.-88G>T
|
|
ENST00000441880.1:n.114-11171G>T
|
|
|
ENST00000464251.5:c.472G>T
|
ENSP00000428980.1:n.472G>T
|
|
ENST00000466323.5:c.546G>T
|
ENSP00000418264.1:p.Leu182=
|
|
ENST00000490775.5:n.331G>T
|
|
|
ENST00000523759.5:n.660G>T
|
|
|
NM_000202.6:c.546G>T
|
NP_000193.1:p.Leu182=
|
|
NM_001166550.2:c.276G>T
|
NP_001160022.1:p.Leu92=
|
|
NM_006123.4:c.546G>T
|
NP_006114.1:p.Leu182=
|
|
NR_104128.1:n.763G>T
|
|
|
NM_000202.7:c.546G>T
|
NP_000193.1:p.Leu182=
|
|
NM_001166550.3:c.276G>T
|
NP_001160022.1:p.Leu92=
|
|
NM_000202.8:c.546G>T
MANE Select
|
NP_000193.1:p.Leu182=
|
|
NM_001166550.4:c.276G>T
|
NP_001160022.1:p.Leu92=
|
|
NM_006123.5:c.546G>T
|
NP_006114.1:p.Leu182=
|
|
NR_104128.2:n.715G>T
|
|
|