ENST00000684241.1:n.1677G>T
|
|
|
ENST00000262186.10:c.844G>T
MANE Select
|
ENSP00000262186.5:p.Ala282Ser
|
|
ENST00000262186.9:c.844G>T
|
ENSP00000262186.5:p.Ala282Ser
|
|
ENST00000430723.4:c.496G>T
|
ENSP00000387657.4:p.Ala166Ser
|
|
ENST00000532957.5:n.1067G>T
|
|
|
NM_000238.3:c.844G>T , LRG_288t1:c.844G>T
|
NP_000229.1:p.Ala282Ser
|
|
NM_172056.2:c.844G>T , LRG_288t2:c.844G>T
|
NP_742053.1:p.Ala282Ser
|
|
XM_011516185.1:c.544G>T
|
XP_011514487.1:p.Ala182Ser
|
|
XM_011516186.1:c.844G>T
|
XP_011514488.1:p.Ala282Ser
|
|
XM_011516185.2:c.544G>T
|
XP_011514487.1:p.Ala182Ser
|
|
XM_011516186.3:c.844G>T
|
XP_011514488.1:p.Ala282Ser
|
|
XM_017012195.1:c.694G>T
|
XP_016867684.1:p.Ala232Ser
|
|
XM_017012196.1:c.667G>T
|
XP_016867685.1:p.Ala223Ser
|
|
NM_000238.4:c.844G>T
MANE Select
|
NP_000229.1:p.Ala282Ser
|
|