ENST00000461280.2:n.1211A>T
|
|
|
ENST00000683359.1:n.37A>T
|
|
|
ENST00000684241.1:n.2746A>T
|
|
|
ENST00000262186.10:c.1913A>T
MANE Select
|
ENSP00000262186.5:p.Lys638Met
|
|
ENST00000330883.9:c.893A>T
|
ENSP00000328531.4:p.Lys298Met
|
|
ENST00000262186.9:c.1913A>T
|
ENSP00000262186.5:p.Lys638Met
|
|
ENST00000330883.8:c.893A>T
|
ENSP00000328531.4:p.Lys298Met
|
|
ENST00000430723.4:c.1565A>T
|
ENSP00000387657.4:p.Lys522Met
|
|
ENST00000461280.1:n.1200A>T
|
|
|
ENST00000473610.5:n.1218A>T
|
|
|
ENST00000532957.5:n.2136A>T
|
|
|
NM_000238.3:c.1913A>T , LRG_288t1:c.1913A>T
|
NP_000229.1:p.Lys638Met
|
|
NM_001204798.1:c.893A>T
|
NP_001191727.1:p.Lys298Met
|
|
NM_172056.2:c.1913A>T , LRG_288t2:c.1913A>T
|
NP_742053.1:p.Lys638Met
|
|
NM_172057.2:c.893A>T , LRG_288t3:c.893A>T
|
NP_742054.1:p.Lys298Met
|
|
XM_011516185.1:c.1613A>T
|
XP_011514487.1:p.Lys538Met
|
|
XM_011516186.1:c.1913A>T
|
XP_011514488.1:p.Lys638Met
|
|
XM_011516185.2:c.1613A>T
|
XP_011514487.1:p.Lys538Met
|
|
XM_011516186.3:c.1913A>T
|
XP_011514488.1:p.Lys638Met
|
|
XM_017012195.1:c.1763A>T
|
XP_016867684.1:p.Lys588Met
|
|
XM_017012196.1:c.1736A>T
|
XP_016867685.1:p.Lys579Met
|
|
NM_000238.4:c.1913A>T
MANE Select
|
NP_000229.1:p.Lys638Met
|
|
NM_001204798.2:c.893A>T
|
NP_001191727.1:p.Lys298Met
|
|
NM_172057.3:c.893A>T
|
NP_742054.1:p.Lys298Met
|
|