ENST00000684241.1:n.1786C>T
|
|
|
ENST00000262186.10:c.953C>T
MANE Select
|
ENSP00000262186.5:p.Ser318Phe
|
|
ENST00000262186.9:c.953C>T
|
ENSP00000262186.5:p.Ser318Phe
|
|
ENST00000430723.4:c.605C>T
|
ENSP00000387657.4:p.Ser202Phe
|
|
ENST00000532957.5:n.1176C>T
|
|
|
NM_000238.3:c.953C>T , LRG_288t1:c.953C>T
|
NP_000229.1:p.Ser318Phe
|
|
NM_172056.2:c.953C>T , LRG_288t2:c.953C>T
|
NP_742053.1:p.Ser318Phe
|
|
XM_011516185.1:c.653C>T
|
XP_011514487.1:p.Ser218Phe
|
|
XM_011516186.1:c.953C>T
|
XP_011514488.1:p.Ser318Phe
|
|
XM_011516185.2:c.653C>T
|
XP_011514487.1:p.Ser218Phe
|
|
XM_011516186.3:c.953C>T
|
XP_011514488.1:p.Ser318Phe
|
|
XM_017012195.1:c.803C>T
|
XP_016867684.1:p.Ser268Phe
|
|
XM_017012196.1:c.776C>T
|
XP_016867685.1:p.Ser259Phe
|
|
NM_000238.4:c.953C>T
MANE Select
|
NP_000229.1:p.Ser318Phe
|
|