ENST00000290866.10:c.2134T>G
MANE Select
|
ENSP00000290866.4:p.Leu712Val
|
|
ENST00000290863.10:c.412T>G
|
ENSP00000290863.6:p.Leu138Val
|
|
ENST00000290866.9:c.2134T>G
|
ENSP00000290866.4:p.Leu712Val
|
|
ENST00000413513.7:c.412T>G
|
ENSP00000392247.3:p.Leu138Val
|
|
ENST00000428043.5:c.2134T>G
|
ENSP00000397593.2:p.Leu712Val
|
|
ENST00000577647.2:c.412T>G
|
ENSP00000464149.1:p.Leu138Val
|
|
ENST00000578839.5:c.*204T>G
|
ENSP00000462110.2:n.*204T>G
|
|
ENST00000579204.1:c.315T>G
|
ENSP00000464629.1:n.315T>G
|
|
ENST00000579314.5:c.412T>G
|
ENSP00000462599.1:p.Leu138Val
|
|
ENST00000579726.5:c.696T>G
|
|
|
ENST00000582005.5:c.*54T>G
|
ENSP00000462002.1:n.*54T>G
|
|
NM_000789.3:c.2134T>G
|
NP_000780.1:p.Leu712Val
|
|
NM_001178057.1:c.412T>G
|
NP_001171528.1:p.Leu138Val
|
|
NM_152830.2:c.412T>G
|
NP_690043.1:p.Leu138Val
|
|
XM_005257110.1:c.1585T>G
|
XP_005257167.1:p.Leu529Val
|
|
XM_006721737.2:c.472T>G
|
XP_006721800.2:p.Leu158Val
|
|
XM_006721737.3:c.472T>G
|
XP_006721800.2:p.Leu158Val
|
|
NM_000789.4:c.2134T>G
MANE Select
|
NP_000780.1:p.Leu712Val
|
|
NM_001178057.2:c.412T>G
|
NP_001171528.1:p.Leu138Val
|
|
NM_152830.3:c.412T>G
|
NP_690043.1:p.Leu138Val
|
|
NM_001382700.1:c.1567T>G
|
NP_001369629.1:p.Leu523Val
|
|
NM_001382701.1:c.1282T>G
|
NP_001369630.1:p.Leu428Val
|
|
NM_001382702.1:c.64T>G
|
NP_001369631.1:p.Leu22Val
|
|
NR_168483.1:n.434T>G
|
|
|