ENST00000290866.10:c.3840C>G
MANE Select
|
ENSP00000290866.4:p.Leu1280=
|
|
ENST00000290863.10:c.2118C>G
|
ENSP00000290863.6:p.Leu706=
|
|
ENST00000290866.9:c.3840C>G
|
ENSP00000290866.4:p.Leu1280=
|
|
ENST00000413513.7:c.1995C>G
|
ENSP00000392247.3:p.Leu665=
|
|
ENST00000428043.5:c.*262C>G
|
ENSP00000397593.2:n.*262C>G
|
|
ENST00000577647.2:c.1969+300C>G
|
ENSP00000464149.1:n.1969+300C>G
|
|
ENST00000578839.5:c.*1595C>G
|
ENSP00000462110.2:n.*1595C>G
|
|
ENST00000579314.5:c.*1569C>G
|
ENSP00000462599.1:n.*1569C>G
|
|
NM_000789.3:c.3840C>G
|
NP_000780.1:p.Leu1280=
|
|
NM_001178057.1:c.1995C>G
|
NP_001171528.1:p.Leu665=
|
|
NM_152830.2:c.2118C>G
|
NP_690043.1:p.Leu706=
|
|
XM_005257110.1:c.3291C>G
|
XP_005257167.1:p.Leu1097=
|
|
XM_006721737.2:c.2178C>G
|
XP_006721800.2:p.Leu726=
|
|
XM_006721737.3:c.2178C>G
|
XP_006721800.2:p.Leu726=
|
|
NM_000789.4:c.3840C>G
MANE Select
|
NP_000780.1:p.Leu1280=
|
|
NM_001178057.2:c.1995C>G
|
NP_001171528.1:p.Leu665=
|
|
NM_152830.3:c.2118C>G
|
NP_690043.1:p.Leu706=
|
|
NM_001382700.1:c.3273C>G
|
NP_001369629.1:p.Leu1091=
|
|
NM_001382701.1:c.2988C>G
|
NP_001369630.1:p.Leu996=
|
|
NM_001382702.1:c.1455C>G
|
NP_001369631.1:p.Leu485=
|
|
NR_168483.1:n.2218C>G
|
|
|