ENST00000340855.11:c.921G=
MANE Select
|
ENSP00000339801.6:p.Leu307=
|
|
ENST00000651111.1:c.288G=
|
ENSP00000498395.1:p.Leu96=
|
|
ENST00000340855.10:c.921G=
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ENSP00000339801.6:p.Leu307=
|
|
ENST00000370441.8:c.921G=
|
ENSP00000359470.4:p.Leu307=
|
|
ENST00000422081.6:c.288G=
|
ENSP00000477056.1:p.Leu96=
|
|
ENST00000441880.1:n.114-3301G=
|
|
|
ENST00000464251.5:c.847G=
|
ENSP00000428980.1:n.847G=
|
|
ENST00000466323.5:c.*112G=
|
ENSP00000418264.1:n.*112G=
|
|
ENST00000490775.5:n.706G=
|
|
|
NM_000202.6:c.921G=
|
NP_000193.1:p.Leu307=
|
|
NM_001166550.2:c.651G=
|
NP_001160022.1:p.Leu217=
|
|
NM_006123.4:c.921G=
|
NP_006114.1:p.Leu307=
|
|
NR_104128.1:n.1268G=
|
|
|
NM_000202.7:c.921G=
|
NP_000193.1:p.Leu307=
|
|
NM_001166550.3:c.651G=
|
NP_001160022.1:p.Leu217=
|
|
NM_000202.8:c.921G=
MANE Select
|
NP_000193.1:p.Leu307=
|
|
NM_001166550.4:c.651G=
|
NP_001160022.1:p.Leu217=
|
|
NM_006123.5:c.921G=
|
NP_006114.1:p.Leu307=
|
|
NR_104128.2:n.1220G=
|
|
|