ENST00000684241.1:n.1859C>A
|
|
|
ENST00000262186.10:c.1026C>A
MANE Select
|
ENSP00000262186.5:p.Asp342Glu
|
|
ENST00000262186.9:c.1026C>A
|
ENSP00000262186.5:p.Asp342Glu
|
|
ENST00000430723.4:c.678C>A
|
ENSP00000387657.4:p.Asp226Glu
|
|
ENST00000532957.5:n.1249C>A
|
|
|
NM_000238.3:c.1026C>A , LRG_288t1:c.1026C>A
|
NP_000229.1:p.Asp342Glu
|
|
NM_172056.2:c.1026C>A , LRG_288t2:c.1026C>A
|
NP_742053.1:p.Asp342Glu
|
|
XM_011516185.1:c.726C>A
|
XP_011514487.1:p.Asp242Glu
|
|
XM_011516186.1:c.1026C>A
|
XP_011514488.1:p.Asp342Glu
|
|
XM_011516185.2:c.726C>A
|
XP_011514487.1:p.Asp242Glu
|
|
XM_011516186.3:c.1026C>A
|
XP_011514488.1:p.Asp342Glu
|
|
XM_017012195.1:c.876C>A
|
XP_016867684.1:p.Asp292Glu
|
|
XM_017012196.1:c.849C>A
|
XP_016867685.1:p.Asp283Glu
|
|
NM_000238.4:c.1026C>A
MANE Select
|
NP_000229.1:p.Asp342Glu
|
|