ENST00000684241.1:n.1790C>T
|
|
|
ENST00000262186.10:c.957C>T
MANE Select
|
ENSP00000262186.5:p.Thr319=
|
|
ENST00000262186.9:c.957C>T
|
ENSP00000262186.5:p.Thr319=
|
|
ENST00000430723.4:c.609C>T
|
ENSP00000387657.4:p.Thr203=
|
|
ENST00000532957.5:n.1180C>T
|
|
|
NM_000238.3:c.957C>T , LRG_288t1:c.957C>T
|
NP_000229.1:p.Thr319=
|
|
NM_172056.2:c.957C>T , LRG_288t2:c.957C>T
|
NP_742053.1:p.Thr319=
|
|
XM_011516185.1:c.657C>T
|
XP_011514487.1:p.Thr219=
|
|
XM_011516186.1:c.957C>T
|
XP_011514488.1:p.Thr319=
|
|
XM_011516185.2:c.657C>T
|
XP_011514487.1:p.Thr219=
|
|
XM_011516186.3:c.957C>T
|
XP_011514488.1:p.Thr319=
|
|
XM_017012195.1:c.807C>T
|
XP_016867684.1:p.Thr269=
|
|
XM_017012196.1:c.780C>T
|
XP_016867685.1:p.Thr260=
|
|
NM_000238.4:c.957C>T
MANE Select
|
NP_000229.1:p.Thr319=
|
|