|
ENST00000461280.2:n.1139C>T
|
|
|
|
ENST00000684241.1:n.2674C>T
|
|
|
|
ENST00000262186.10:c.1841C>T
MANE Select
|
ENSP00000262186.5:p.Ala614Val
|
|
|
ENST00000330883.9:c.821C>T
|
ENSP00000328531.4:p.Ala274Val
|
|
|
ENST00000262186.9:c.1841C>T
|
ENSP00000262186.5:p.Ala614Val
|
|
|
ENST00000330883.8:c.821C>T
|
ENSP00000328531.4:p.Ala274Val
|
|
|
ENST00000430723.4:c.1493C>T
|
ENSP00000387657.4:p.Ala498Val
|
|
|
ENST00000461280.1:n.1128C>T
|
|
|
|
ENST00000473610.5:n.1146C>T
|
|
|
|
ENST00000532957.5:n.2064C>T
|
|
|
|
NM_000238.3:c.1841C>T , LRG_288t1:c.1841C>T
|
NP_000229.1:p.Ala614Val
|
|
|
NM_001204798.1:c.821C>T
|
NP_001191727.1:p.Ala274Val
|
|
|
NM_172056.2:c.1841C>T , LRG_288t2:c.1841C>T
|
NP_742053.1:p.Ala614Val
|
|
|
NM_172057.2:c.821C>T , LRG_288t3:c.821C>T
|
NP_742054.1:p.Ala274Val
|
|
|
XM_011516185.1:c.1541C>T
|
XP_011514487.1:p.Ala514Val
|
|
|
XM_011516186.1:c.1841C>T
|
XP_011514488.1:p.Ala614Val
|
|
|
XM_011516185.2:c.1541C>T
|
XP_011514487.1:p.Ala514Val
|
|
|
XM_011516186.3:c.1841C>T
|
XP_011514488.1:p.Ala614Val
|
|
|
XM_017012195.1:c.1691C>T
|
XP_016867684.1:p.Ala564Val
|
|
|
XM_017012196.1:c.1664C>T
|
XP_016867685.1:p.Ala555Val
|
|
|
NM_000238.4:c.1841C>T
MANE Select
|
NP_000229.1:p.Ala614Val
|
|
|
NM_001204798.2:c.821C>T
|
NP_001191727.1:p.Ala274Val
|
|
|
NM_172057.3:c.821C>T
|
NP_742054.1:p.Ala274Val
|
|
