ENST00000339077.10:c.1263C>A
MANE Select
|
ENSP00000343273.4:p.Cys421Ter
|
|
ENST00000339077.9:c.1263C>A
|
ENSP00000343273.4:p.Cys421Ter
|
|
ENST00000409689.5:c.1119C>A
|
ENSP00000386263.1:p.Cys373Ter
|
|
ENST00000469576.1:n.150C>A
|
|
|
ENST00000521082.5:c.*1271C>A
|
ENSP00000430351.1:n.*1271C>A
|
|
NM_001031710.2:c.1263C>A
|
NP_001026880.2:p.Cys421Ter
|
|
NM_018846.4:c.1119C>A
|
NP_061334.4:p.Cys373Ter
|
|
NR_033328.1:n.1687C>A
|
|
|
XM_006715753.1:c.1302C>A
|
XP_006715816.1:p.Cys434Ter
|
|
XM_006715754.1:c.1236C>A
|
XP_006715817.1:p.Cys412Ter
|
|
XM_006715755.1:c.1236C>A
|
XP_006715818.1:p.Cys412Ter
|
|
XM_006715756.1:c.1158C>A
|
XP_006715819.1:p.Cys386Ter
|
|
XM_006715753.3:c.1302C>A
|
XP_006715816.1:p.Cys434Ter
|
|
XM_006715754.3:c.1236C>A
|
XP_006715817.1:p.Cys412Ter
|
|
XM_006715755.3:c.1236C>A
|
XP_006715818.1:p.Cys412Ter
|
|
XM_006715756.3:c.1158C>A
|
XP_006715819.1:p.Cys386Ter
|
|
XM_017012439.2:c.1197C>A
|
XP_016867928.1:p.Cys399Ter
|
|
NM_001031710.3:c.1263C>A
MANE Select
|
NP_001026880.2:p.Cys421Ter
|
|
NM_018846.5:c.1119C>A
|
NP_061334.4:p.Cys373Ter
|
|
NR_033328.2:n.1636C>A
|
|
|