ENST00000461280.2:n.685T>G
|
|
|
ENST00000684116.1:n.280T>G
|
|
|
ENST00000684241.1:n.2220T>G
|
|
|
ENST00000262186.10:c.1387T>G
MANE Select
|
ENSP00000262186.5:p.Phe463Val
|
|
ENST00000330883.9:c.367T>G
|
ENSP00000328531.4:p.Phe123Val
|
|
ENST00000262186.9:c.1387T>G
|
ENSP00000262186.5:p.Phe463Val
|
|
ENST00000330883.8:c.367T>G
|
ENSP00000328531.4:p.Phe123Val
|
|
ENST00000430723.4:c.1039T>G
|
ENSP00000387657.4:p.Phe347Val
|
|
ENST00000461280.1:n.674T>G
|
|
|
ENST00000473610.5:n.692T>G
|
|
|
ENST00000532957.5:n.1610T>G
|
|
|
NM_000238.3:c.1387T>G , LRG_288t1:c.1387T>G
|
NP_000229.1:p.Phe463Val
|
|
NM_001204798.1:c.367T>G
|
NP_001191727.1:p.Phe123Val
|
|
NM_172056.2:c.1387T>G , LRG_288t2:c.1387T>G
|
NP_742053.1:p.Phe463Val
|
|
NM_172057.2:c.367T>G , LRG_288t3:c.367T>G
|
NP_742054.1:p.Phe123Val
|
|
XM_011516185.1:c.1087T>G
|
XP_011514487.1:p.Phe363Val
|
|
XM_011516186.1:c.1387T>G
|
XP_011514488.1:p.Phe463Val
|
|
XM_011516185.2:c.1087T>G
|
XP_011514487.1:p.Phe363Val
|
|
XM_011516186.3:c.1387T>G
|
XP_011514488.1:p.Phe463Val
|
|
XM_017012195.1:c.1237T>G
|
XP_016867684.1:p.Phe413Val
|
|
XM_017012196.1:c.1210T>G
|
XP_016867685.1:p.Phe404Val
|
|
NM_000238.4:c.1387T>G
MANE Select
|
NP_000229.1:p.Phe463Val
|
|
NM_001204798.2:c.367T>G
|
NP_001191727.1:p.Phe123Val
|
|
NM_172057.3:c.367T>G
|
NP_742054.1:p.Phe123Val
|
|