ENST00000684241.1:n.1938A>T
|
|
|
ENST00000262186.10:c.1105A>T
MANE Select
|
ENSP00000262186.5:p.Asn369Tyr
|
|
ENST00000262186.9:c.1105A>T
|
ENSP00000262186.5:p.Asn369Tyr
|
|
ENST00000430723.4:c.757A>T
|
ENSP00000387657.4:p.Asn253Tyr
|
|
ENST00000532957.5:n.1328A>T
|
|
|
NM_000238.3:c.1105A>T , LRG_288t1:c.1105A>T
|
NP_000229.1:p.Asn369Tyr
|
|
NM_172056.2:c.1105A>T , LRG_288t2:c.1105A>T
|
NP_742053.1:p.Asn369Tyr
|
|
XM_011516185.1:c.805A>T
|
XP_011514487.1:p.Asn269Tyr
|
|
XM_011516186.1:c.1105A>T
|
XP_011514488.1:p.Asn369Tyr
|
|
XM_011516185.2:c.805A>T
|
XP_011514487.1:p.Asn269Tyr
|
|
XM_011516186.3:c.1105A>T
|
XP_011514488.1:p.Asn369Tyr
|
|
XM_017012195.1:c.955A>T
|
XP_016867684.1:p.Asn319Tyr
|
|
XM_017012196.1:c.928A>T
|
XP_016867685.1:p.Asn310Tyr
|
|
NM_000238.4:c.1105A>T
MANE Select
|
NP_000229.1:p.Asn369Tyr
|
|