ENST00000461280.2:n.703A>G
|
|
|
ENST00000684116.1:n.298A>G
|
|
|
ENST00000684241.1:n.2238A>G
|
|
|
ENST00000262186.10:c.1405A>G
MANE Select
|
ENSP00000262186.5:p.Ile469Val
|
|
ENST00000330883.9:c.385A>G
|
ENSP00000328531.4:p.Ile129Val
|
|
ENST00000262186.9:c.1405A>G
|
ENSP00000262186.5:p.Ile469Val
|
|
ENST00000330883.8:c.385A>G
|
ENSP00000328531.4:p.Ile129Val
|
|
ENST00000430723.4:c.1057A>G
|
ENSP00000387657.4:p.Ile353Val
|
|
ENST00000461280.1:n.692A>G
|
|
|
ENST00000473610.5:n.710A>G
|
|
|
ENST00000532957.5:n.1628A>G
|
|
|
NM_000238.3:c.1405A>G , LRG_288t1:c.1405A>G
|
NP_000229.1:p.Ile469Val
|
|
NM_001204798.1:c.385A>G
|
NP_001191727.1:p.Ile129Val
|
|
NM_172056.2:c.1405A>G , LRG_288t2:c.1405A>G
|
NP_742053.1:p.Ile469Val
|
|
NM_172057.2:c.385A>G , LRG_288t3:c.385A>G
|
NP_742054.1:p.Ile129Val
|
|
XM_011516185.1:c.1105A>G
|
XP_011514487.1:p.Ile369Val
|
|
XM_011516186.1:c.1405A>G
|
XP_011514488.1:p.Ile469Val
|
|
XM_011516185.2:c.1105A>G
|
XP_011514487.1:p.Ile369Val
|
|
XM_011516186.3:c.1405A>G
|
XP_011514488.1:p.Ile469Val
|
|
XM_017012195.1:c.1255A>G
|
XP_016867684.1:p.Ile419Val
|
|
XM_017012196.1:c.1228A>G
|
XP_016867685.1:p.Ile410Val
|
|
NM_000238.4:c.1405A>G
MANE Select
|
NP_000229.1:p.Ile469Val
|
|
NM_001204798.2:c.385A>G
|
NP_001191727.1:p.Ile129Val
|
|
NM_172057.3:c.385A>G
|
NP_742054.1:p.Ile129Val
|
|