ENST00000262186.10:c.149A>T
MANE Select
|
ENSP00000262186.5:p.Glu50Val
|
|
ENST00000262186.9:c.149A>T
|
ENSP00000262186.5:p.Glu50Val
|
|
ENST00000430723.4:c.-29A>T
|
ENSP00000387657.4:n.-29A>T
|
|
ENST00000532957.5:n.372A>T
|
|
|
NM_000238.3:c.149A>T , LRG_288t1:c.149A>T
|
NP_000229.1:p.Glu50Val
|
|
NM_172056.2:c.149A>T , LRG_288t2:c.149A>T
|
NP_742053.1:p.Glu50Val
|
|
XM_011516186.1:c.149A>T
|
XP_011514488.1:p.Glu50Val
|
|
XM_011516186.3:c.149A>T
|
XP_011514488.1:p.Glu50Val
|
|
XM_017012196.1:c.-29A>T
|
XP_016867685.1:n.-29A>T
|
|
NM_000238.4:c.149A>T
MANE Select
|
NP_000229.1:p.Glu50Val
|
|