ENST00000684241.1:n.1948A>T
|
|
|
ENST00000262186.10:c.1115A>T
MANE Select
|
ENSP00000262186.5:p.Glu372Val
|
|
ENST00000262186.9:c.1115A>T
|
ENSP00000262186.5:p.Glu372Val
|
|
ENST00000430723.4:c.767A>T
|
ENSP00000387657.4:p.Glu256Val
|
|
ENST00000532957.5:n.1338A>T
|
|
|
NM_000238.3:c.1115A>T , LRG_288t1:c.1115A>T
|
NP_000229.1:p.Glu372Val
|
|
NM_172056.2:c.1115A>T , LRG_288t2:c.1115A>T
|
NP_742053.1:p.Glu372Val
|
|
XM_011516185.1:c.815A>T
|
XP_011514487.1:p.Glu272Val
|
|
XM_011516186.1:c.1115A>T
|
XP_011514488.1:p.Glu372Val
|
|
XM_011516185.2:c.815A>T
|
XP_011514487.1:p.Glu272Val
|
|
XM_011516186.3:c.1115A>T
|
XP_011514488.1:p.Glu372Val
|
|
XM_017012195.1:c.965A>T
|
XP_016867684.1:p.Glu322Val
|
|
XM_017012196.1:c.938A>T
|
XP_016867685.1:p.Glu313Val
|
|
NM_000238.4:c.1115A>T
MANE Select
|
NP_000229.1:p.Glu372Val
|
|