ENST00000461280.2:n.652C>G
|
|
|
ENST00000684116.1:n.247C>G
|
|
|
ENST00000684241.1:n.2187C>G
|
|
|
ENST00000262186.10:c.1354C>G
MANE Select
|
ENSP00000262186.5:p.Leu452Val
|
|
ENST00000330883.9:c.334C>G
|
ENSP00000328531.4:p.Leu112Val
|
|
ENST00000262186.9:c.1354C>G
|
ENSP00000262186.5:p.Leu452Val
|
|
ENST00000330883.8:c.334C>G
|
ENSP00000328531.4:p.Leu112Val
|
|
ENST00000430723.4:c.1006C>G
|
ENSP00000387657.4:p.Leu336Val
|
|
ENST00000461280.1:n.641C>G
|
|
|
ENST00000473610.5:n.659C>G
|
|
|
ENST00000532957.5:n.1577C>G
|
|
|
NM_000238.3:c.1354C>G , LRG_288t1:c.1354C>G
|
NP_000229.1:p.Leu452Val
|
|
NM_001204798.1:c.334C>G
|
NP_001191727.1:p.Leu112Val
|
|
NM_172056.2:c.1354C>G , LRG_288t2:c.1354C>G
|
NP_742053.1:p.Leu452Val
|
|
NM_172057.2:c.334C>G , LRG_288t3:c.334C>G
|
NP_742054.1:p.Leu112Val
|
|
XM_011516185.1:c.1054C>G
|
XP_011514487.1:p.Leu352Val
|
|
XM_011516186.1:c.1354C>G
|
XP_011514488.1:p.Leu452Val
|
|
XM_011516185.2:c.1054C>G
|
XP_011514487.1:p.Leu352Val
|
|
XM_011516186.3:c.1354C>G
|
XP_011514488.1:p.Leu452Val
|
|
XM_017012195.1:c.1204C>G
|
XP_016867684.1:p.Leu402Val
|
|
XM_017012196.1:c.1177C>G
|
XP_016867685.1:p.Leu393Val
|
|
NM_000238.4:c.1354C>G
MANE Select
|
NP_000229.1:p.Leu452Val
|
|
NM_001204798.2:c.334C>G
|
NP_001191727.1:p.Leu112Val
|
|
NM_172057.3:c.334C>G
|
NP_742054.1:p.Leu112Val
|
|