ENST00000461280.2:n.1526T>C
|
|
|
ENST00000684241.1:n.3061T>C
|
|
|
ENST00000262186.10:c.2228T>C
MANE Select
|
ENSP00000262186.5:p.Phe743Ser
|
|
ENST00000330883.9:c.1208T>C
|
ENSP00000328531.4:p.Phe403Ser
|
|
ENST00000262186.9:c.2228T>C
|
ENSP00000262186.5:p.Phe743Ser
|
|
ENST00000330883.8:c.1208T>C
|
ENSP00000328531.4:p.Phe403Ser
|
|
ENST00000430723.4:c.1880T>C
|
ENSP00000387657.4:p.Phe627Ser
|
|
ENST00000461280.1:n.1515T>C
|
|
|
ENST00000473610.5:n.1860T>C
|
|
|
ENST00000532957.5:n.2451T>C
|
|
|
NM_000238.3:c.2228T>C , LRG_288t1:c.2228T>C
|
NP_000229.1:p.Phe743Ser
|
|
NM_001204798.1:c.1208T>C
|
NP_001191727.1:p.Phe403Ser
|
|
NM_172056.2:c.2228T>C , LRG_288t2:c.2228T>C
|
NP_742053.1:p.Phe743Ser
|
|
NM_172057.2:c.1208T>C , LRG_288t3:c.1208T>C
|
NP_742054.1:p.Phe403Ser
|
|
XM_011516185.1:c.1928T>C
|
XP_011514487.1:p.Phe643Ser
|
|
XM_011516186.1:c.2228T>C
|
XP_011514488.1:p.Phe743Ser
|
|
XM_011516185.2:c.1928T>C
|
XP_011514487.1:p.Phe643Ser
|
|
XM_011516186.3:c.2228T>C
|
XP_011514488.1:p.Phe743Ser
|
|
XM_017012195.1:c.2078T>C
|
XP_016867684.1:p.Phe693Ser
|
|
XM_017012196.1:c.2051T>C
|
XP_016867685.1:p.Phe684Ser
|
|
NM_000238.4:c.2228T>C
MANE Select
|
NP_000229.1:p.Phe743Ser
|
|
NM_001204798.2:c.1208T>C
|
NP_001191727.1:p.Phe403Ser
|
|
NM_172057.3:c.1208T>C
|
NP_742054.1:p.Phe403Ser
|
|