ENST00000339077.10:c.948G>C
MANE Select
|
ENSP00000343273.4:p.Trp316Cys
|
|
ENST00000339077.9:c.948G>C
|
ENSP00000343273.4:p.Trp316Cys
|
|
ENST00000409689.5:c.804G>C
|
ENSP00000386263.1:p.Trp268Cys
|
|
ENST00000521082.5:c.*956G>C
|
ENSP00000430351.1:n.*956G>C
|
|
NM_001031710.2:c.948G>C
|
NP_001026880.2:p.Trp316Cys
|
|
NM_018846.4:c.804G>C
|
NP_061334.4:p.Trp268Cys
|
|
NR_033328.1:n.1372G>C
|
|
|
XM_006715753.1:c.987G>C
|
XP_006715816.1:p.Trp329Cys
|
|
XM_006715754.1:c.921G>C
|
XP_006715817.1:p.Trp307Cys
|
|
XM_006715755.1:c.921G>C
|
XP_006715818.1:p.Trp307Cys
|
|
XM_006715756.1:c.843G>C
|
XP_006715819.1:p.Trp281Cys
|
|
XM_006715753.3:c.987G>C
|
XP_006715816.1:p.Trp329Cys
|
|
XM_006715754.3:c.921G>C
|
XP_006715817.1:p.Trp307Cys
|
|
XM_006715755.3:c.921G>C
|
XP_006715818.1:p.Trp307Cys
|
|
XM_006715756.3:c.843G>C
|
XP_006715819.1:p.Trp281Cys
|
|
XM_017012439.2:c.882G>C
|
XP_016867928.1:p.Trp294Cys
|
|
NM_001031710.3:c.948G>C
MANE Select
|
NP_001026880.2:p.Trp316Cys
|
|
NM_018846.5:c.804G>C
|
NP_061334.4:p.Trp268Cys
|
|
NR_033328.2:n.1321G>C
|
|
|