ENST00000461280.2:n.1067G>T
|
|
|
ENST00000684241.1:n.2602G>T
|
|
|
ENST00000262186.10:c.1769G>T
MANE Select
|
ENSP00000262186.5:p.Gly590Val
|
|
ENST00000330883.9:c.749G>T
|
ENSP00000328531.4:p.Gly250Val
|
|
ENST00000262186.9:c.1769G>T
|
ENSP00000262186.5:p.Gly590Val
|
|
ENST00000330883.8:c.749G>T
|
ENSP00000328531.4:p.Gly250Val
|
|
ENST00000430723.4:c.1421G>T
|
ENSP00000387657.4:p.Gly474Val
|
|
ENST00000461280.1:n.1056G>T
|
|
|
ENST00000473610.5:n.1074G>T
|
|
|
ENST00000532957.5:n.1992G>T
|
|
|
NM_000238.3:c.1769G>T , LRG_288t1:c.1769G>T
|
NP_000229.1:p.Gly590Val
|
|
NM_001204798.1:c.749G>T
|
NP_001191727.1:p.Gly250Val
|
|
NM_172056.2:c.1769G>T , LRG_288t2:c.1769G>T
|
NP_742053.1:p.Gly590Val
|
|
NM_172057.2:c.749G>T , LRG_288t3:c.749G>T
|
NP_742054.1:p.Gly250Val
|
|
XM_011516185.1:c.1469G>T
|
XP_011514487.1:p.Gly490Val
|
|
XM_011516186.1:c.1769G>T
|
XP_011514488.1:p.Gly590Val
|
|
XM_011516185.2:c.1469G>T
|
XP_011514487.1:p.Gly490Val
|
|
XM_011516186.3:c.1769G>T
|
XP_011514488.1:p.Gly590Val
|
|
XM_017012195.1:c.1619G>T
|
XP_016867684.1:p.Gly540Val
|
|
XM_017012196.1:c.1592G>T
|
XP_016867685.1:p.Gly531Val
|
|
NM_000238.4:c.1769G>T
MANE Select
|
NP_000229.1:p.Gly590Val
|
|
NM_001204798.2:c.749G>T
|
NP_001191727.1:p.Gly250Val
|
|
NM_172057.3:c.749G>T
|
NP_742054.1:p.Gly250Val
|
|