ENST00000339077.10:c.937G>T
MANE Select
|
ENSP00000343273.4:p.Asp313Tyr
|
|
ENST00000339077.9:c.937G>T
|
ENSP00000343273.4:p.Asp313Tyr
|
|
ENST00000409689.5:c.793G>T
|
ENSP00000386263.1:p.Asp265Tyr
|
|
ENST00000521082.5:c.*945G>T
|
ENSP00000430351.1:n.*945G>T
|
|
NM_001031710.2:c.937G>T
|
NP_001026880.2:p.Asp313Tyr
|
|
NM_018846.4:c.793G>T
|
NP_061334.4:p.Asp265Tyr
|
|
NR_033328.1:n.1361G>T
|
|
|
XM_006715753.1:c.976G>T
|
XP_006715816.1:p.Asp326Tyr
|
|
XM_006715754.1:c.910G>T
|
XP_006715817.1:p.Asp304Tyr
|
|
XM_006715755.1:c.910G>T
|
XP_006715818.1:p.Asp304Tyr
|
|
XM_006715756.1:c.832G>T
|
XP_006715819.1:p.Asp278Tyr
|
|
XM_006715753.3:c.976G>T
|
XP_006715816.1:p.Asp326Tyr
|
|
XM_006715754.3:c.910G>T
|
XP_006715817.1:p.Asp304Tyr
|
|
XM_006715755.3:c.910G>T
|
XP_006715818.1:p.Asp304Tyr
|
|
XM_006715756.3:c.832G>T
|
XP_006715819.1:p.Asp278Tyr
|
|
XM_017012439.2:c.871G>T
|
XP_016867928.1:p.Asp291Tyr
|
|
NM_001031710.3:c.937G>T
MANE Select
|
NP_001026880.2:p.Asp313Tyr
|
|
NM_018846.5:c.793G>T
|
NP_061334.4:p.Asp265Tyr
|
|
NR_033328.2:n.1310G>T
|
|
|