ENST00000684241.1:n.1606C>A
|
|
|
ENST00000262186.10:c.773C>A
MANE Select
|
ENSP00000262186.5:p.Pro258His
|
|
ENST00000262186.9:c.773C>A
|
ENSP00000262186.5:p.Pro258His
|
|
ENST00000430723.4:c.425C>A
|
ENSP00000387657.4:p.Pro142His
|
|
ENST00000532957.5:n.996C>A
|
|
|
NM_000238.3:c.773C>A , LRG_288t1:c.773C>A
|
NP_000229.1:p.Pro258His
|
|
NM_172056.2:c.773C>A , LRG_288t2:c.773C>A
|
NP_742053.1:p.Pro258His
|
|
XM_011516185.1:c.473C>A
|
XP_011514487.1:p.Pro158His
|
|
XM_011516186.1:c.773C>A
|
XP_011514488.1:p.Pro258His
|
|
XM_011516185.2:c.473C>A
|
XP_011514487.1:p.Pro158His
|
|
XM_011516186.3:c.773C>A
|
XP_011514488.1:p.Pro258His
|
|
XM_017012195.1:c.623C>A
|
XP_016867684.1:p.Pro208His
|
|
XM_017012196.1:c.596C>A
|
XP_016867685.1:p.Pro199His
|
|
NM_000238.4:c.773C>A
MANE Select
|
NP_000229.1:p.Pro258His
|
|