ENST00000684241.1:n.3918A>T
|
|
|
ENST00000262186.10:c.3085A>T
MANE Select
|
ENSP00000262186.5:p.Ser1029Cys
|
|
ENST00000330883.9:c.2065A>T
|
ENSP00000328531.4:p.Ser689Cys
|
|
ENST00000262186.9:c.3085A>T
|
ENSP00000262186.5:p.Ser1029Cys
|
|
ENST00000330883.8:c.2065A>T
|
ENSP00000328531.4:p.Ser689Cys
|
|
NM_000238.3:c.3085A>T , LRG_288t1:c.3085A>T
|
NP_000229.1:p.Ser1029Cys
|
|
NM_172057.2:c.2065A>T , LRG_288t3:c.2065A>T
|
NP_742054.1:p.Ser689Cys
|
|
XM_011516185.1:c.2785A>T
|
XP_011514487.1:p.Ser929Cys
|
|
XM_011516185.2:c.2785A>T
|
XP_011514487.1:p.Ser929Cys
|
|
XM_017012195.1:c.2935A>T
|
XP_016867684.1:p.Ser979Cys
|
|
XM_017012196.1:c.2908A>T
|
XP_016867685.1:p.Ser970Cys
|
|
NM_000238.4:c.3085A>T
MANE Select
|
NP_000229.1:p.Ser1029Cys
|
|
NM_172057.3:c.2065A>T
|
NP_742054.1:p.Ser689Cys
|
|