ENST00000339077.10:c.1170A>T
MANE Select
|
ENSP00000343273.4:p.Ser390=
|
|
ENST00000339077.9:c.1170A>T
|
ENSP00000343273.4:p.Ser390=
|
|
ENST00000409689.5:c.1026A>T
|
ENSP00000386263.1:p.Ser342=
|
|
ENST00000469576.1:n.57A>T
|
|
|
ENST00000521082.5:c.*1178A>T
|
ENSP00000430351.1:n.*1178A>T
|
|
NM_001031710.2:c.1170A>T
|
NP_001026880.2:p.Ser390=
|
|
NM_018846.4:c.1026A>T
|
NP_061334.4:p.Ser342=
|
|
NR_033328.1:n.1594A>T
|
|
|
XM_006715753.1:c.1209A>T
|
XP_006715816.1:p.Ser403=
|
|
XM_006715754.1:c.1143A>T
|
XP_006715817.1:p.Ser381=
|
|
XM_006715755.1:c.1143A>T
|
XP_006715818.1:p.Ser381=
|
|
XM_006715756.1:c.1065A>T
|
XP_006715819.1:p.Ser355=
|
|
XM_006715753.3:c.1209A>T
|
XP_006715816.1:p.Ser403=
|
|
XM_006715754.3:c.1143A>T
|
XP_006715817.1:p.Ser381=
|
|
XM_006715755.3:c.1143A>T
|
XP_006715818.1:p.Ser381=
|
|
XM_006715756.3:c.1065A>T
|
XP_006715819.1:p.Ser355=
|
|
XM_017012439.2:c.1104A>T
|
XP_016867928.1:p.Ser368=
|
|
NM_001031710.3:c.1170A>T
MANE Select
|
NP_001026880.2:p.Ser390=
|
|
NM_018846.5:c.1026A>T
|
NP_061334.4:p.Ser342=
|
|
NR_033328.2:n.1543A>T
|
|
|