ENST00000684241.1:n.1692G>C
|
|
|
ENST00000262186.10:c.859G>C
MANE Select
|
ENSP00000262186.5:p.Asp287His
|
|
ENST00000262186.9:c.859G>C
|
ENSP00000262186.5:p.Asp287His
|
|
ENST00000430723.4:c.511G>C
|
ENSP00000387657.4:p.Asp171His
|
|
ENST00000532957.5:n.1082G>C
|
|
|
NM_000238.3:c.859G>C , LRG_288t1:c.859G>C
|
NP_000229.1:p.Asp287His
|
|
NM_172056.2:c.859G>C , LRG_288t2:c.859G>C
|
NP_742053.1:p.Asp287His
|
|
XM_011516185.1:c.559G>C
|
XP_011514487.1:p.Asp187His
|
|
XM_011516186.1:c.859G>C
|
XP_011514488.1:p.Asp287His
|
|
XM_011516185.2:c.559G>C
|
XP_011514487.1:p.Asp187His
|
|
XM_011516186.3:c.859G>C
|
XP_011514488.1:p.Asp287His
|
|
XM_017012195.1:c.709G>C
|
XP_016867684.1:p.Asp237His
|
|
XM_017012196.1:c.682G>C
|
XP_016867685.1:p.Asp228His
|
|
NM_000238.4:c.859G>C
MANE Select
|
NP_000229.1:p.Asp287His
|
|