ENST00000461280.2:n.1661A>C
|
|
|
ENST00000684241.1:n.3196A>C
|
|
|
ENST00000262186.10:c.2363A>C
MANE Select
|
ENSP00000262186.5:p.Glu788Ala
|
|
ENST00000330883.9:c.1343A>C
|
ENSP00000328531.4:p.Glu448Ala
|
|
ENST00000262186.9:c.2363A>C
|
ENSP00000262186.5:p.Glu788Ala
|
|
ENST00000330883.8:c.1343A>C
|
ENSP00000328531.4:p.Glu448Ala
|
|
ENST00000430723.4:c.2015A>C
|
ENSP00000387657.4:p.Glu672Ala
|
|
ENST00000461280.1:n.1650A>C
|
|
|
ENST00000473610.5:n.1995A>C
|
|
|
ENST00000532957.5:n.2586A>C
|
|
|
NM_000238.3:c.2363A>C , LRG_288t1:c.2363A>C
|
NP_000229.1:p.Glu788Ala
|
|
NM_001204798.1:c.1343A>C
|
NP_001191727.1:p.Glu448Ala
|
|
NM_172056.2:c.2363A>C , LRG_288t2:c.2363A>C
|
NP_742053.1:p.Glu788Ala
|
|
NM_172057.2:c.1343A>C , LRG_288t3:c.1343A>C
|
NP_742054.1:p.Glu448Ala
|
|
XM_011516185.1:c.2063A>C
|
XP_011514487.1:p.Glu688Ala
|
|
XM_011516186.1:c.2363A>C
|
XP_011514488.1:p.Glu788Ala
|
|
XM_011516185.2:c.2063A>C
|
XP_011514487.1:p.Glu688Ala
|
|
XM_011516186.3:c.2363A>C
|
XP_011514488.1:p.Glu788Ala
|
|
XM_017012195.1:c.2213A>C
|
XP_016867684.1:p.Glu738Ala
|
|
XM_017012196.1:c.2186A>C
|
XP_016867685.1:p.Glu729Ala
|
|
NM_000238.4:c.2363A>C
MANE Select
|
NP_000229.1:p.Glu788Ala
|
|
NM_001204798.2:c.1343A>C
|
NP_001191727.1:p.Glu448Ala
|
|
NM_172057.3:c.1343A>C
|
NP_742054.1:p.Glu448Ala
|
|