ENST00000339077.10:c.952G>T
MANE Select
|
ENSP00000343273.4:p.Asp318Tyr
|
|
ENST00000339077.9:c.952G>T
|
ENSP00000343273.4:p.Asp318Tyr
|
|
ENST00000409689.5:c.808G>T
|
ENSP00000386263.1:p.Asp270Tyr
|
|
ENST00000521082.5:c.*960G>T
|
ENSP00000430351.1:n.*960G>T
|
|
NM_001031710.2:c.952G>T
|
NP_001026880.2:p.Asp318Tyr
|
|
NM_018846.4:c.808G>T
|
NP_061334.4:p.Asp270Tyr
|
|
NR_033328.1:n.1376G>T
|
|
|
XM_006715753.1:c.991G>T
|
XP_006715816.1:p.Asp331Tyr
|
|
XM_006715754.1:c.925G>T
|
XP_006715817.1:p.Asp309Tyr
|
|
XM_006715755.1:c.925G>T
|
XP_006715818.1:p.Asp309Tyr
|
|
XM_006715756.1:c.847G>T
|
XP_006715819.1:p.Asp283Tyr
|
|
XM_006715753.3:c.991G>T
|
XP_006715816.1:p.Asp331Tyr
|
|
XM_006715754.3:c.925G>T
|
XP_006715817.1:p.Asp309Tyr
|
|
XM_006715755.3:c.925G>T
|
XP_006715818.1:p.Asp309Tyr
|
|
XM_006715756.3:c.847G>T
|
XP_006715819.1:p.Asp283Tyr
|
|
XM_017012439.2:c.886G>T
|
XP_016867928.1:p.Asp296Tyr
|
|
NM_001031710.3:c.952G>T
MANE Select
|
NP_001026880.2:p.Asp318Tyr
|
|
NM_018846.5:c.808G>T
|
NP_061334.4:p.Asp270Tyr
|
|
NR_033328.2:n.1325G>T
|
|
|