ENST00000461280.2:n.1201A>T
|
|
|
ENST00000683359.1:n.27A>T
|
|
|
ENST00000684241.1:n.2736A>T
|
|
|
ENST00000262186.10:c.1903A>T
MANE Select
|
ENSP00000262186.5:p.Asn635Tyr
|
|
ENST00000330883.9:c.883A>T
|
ENSP00000328531.4:p.Asn295Tyr
|
|
ENST00000262186.9:c.1903A>T
|
ENSP00000262186.5:p.Asn635Tyr
|
|
ENST00000330883.8:c.883A>T
|
ENSP00000328531.4:p.Asn295Tyr
|
|
ENST00000430723.4:c.1555A>T
|
ENSP00000387657.4:p.Asn519Tyr
|
|
ENST00000461280.1:n.1190A>T
|
|
|
ENST00000473610.5:n.1208A>T
|
|
|
ENST00000532957.5:n.2126A>T
|
|
|
NM_000238.3:c.1903A>T , LRG_288t1:c.1903A>T
|
NP_000229.1:p.Asn635Tyr
|
|
NM_001204798.1:c.883A>T
|
NP_001191727.1:p.Asn295Tyr
|
|
NM_172056.2:c.1903A>T , LRG_288t2:c.1903A>T
|
NP_742053.1:p.Asn635Tyr
|
|
NM_172057.2:c.883A>T , LRG_288t3:c.883A>T
|
NP_742054.1:p.Asn295Tyr
|
|
XM_011516185.1:c.1603A>T
|
XP_011514487.1:p.Asn535Tyr
|
|
XM_011516186.1:c.1903A>T
|
XP_011514488.1:p.Asn635Tyr
|
|
XM_011516185.2:c.1603A>T
|
XP_011514487.1:p.Asn535Tyr
|
|
XM_011516186.3:c.1903A>T
|
XP_011514488.1:p.Asn635Tyr
|
|
XM_017012195.1:c.1753A>T
|
XP_016867684.1:p.Asn585Tyr
|
|
XM_017012196.1:c.1726A>T
|
XP_016867685.1:p.Asn576Tyr
|
|
NM_000238.4:c.1903A>T
MANE Select
|
NP_000229.1:p.Asn635Tyr
|
|
NM_001204798.2:c.883A>T
|
NP_001191727.1:p.Asn295Tyr
|
|
NM_172057.3:c.883A>T
|
NP_742054.1:p.Asn295Tyr
|
|