ENST00000684241.1:n.1785T>A
|
|
|
ENST00000262186.10:c.952T>A
MANE Select
|
ENSP00000262186.5:p.Ser318Thr
|
|
ENST00000262186.9:c.952T>A
|
ENSP00000262186.5:p.Ser318Thr
|
|
ENST00000430723.4:c.604T>A
|
ENSP00000387657.4:p.Ser202Thr
|
|
ENST00000532957.5:n.1175T>A
|
|
|
NM_000238.3:c.952T>A , LRG_288t1:c.952T>A
|
NP_000229.1:p.Ser318Thr
|
|
NM_172056.2:c.952T>A , LRG_288t2:c.952T>A
|
NP_742053.1:p.Ser318Thr
|
|
XM_011516185.1:c.652T>A
|
XP_011514487.1:p.Ser218Thr
|
|
XM_011516186.1:c.952T>A
|
XP_011514488.1:p.Ser318Thr
|
|
XM_011516185.2:c.652T>A
|
XP_011514487.1:p.Ser218Thr
|
|
XM_011516186.3:c.952T>A
|
XP_011514488.1:p.Ser318Thr
|
|
XM_017012195.1:c.802T>A
|
XP_016867684.1:p.Ser268Thr
|
|
XM_017012196.1:c.775T>A
|
XP_016867685.1:p.Ser259Thr
|
|
NM_000238.4:c.952T>A
MANE Select
|
NP_000229.1:p.Ser318Thr
|
|