ENST00000339077.10:c.963C>G
MANE Select
|
ENSP00000343273.4:p.Cys321Trp
|
|
ENST00000339077.9:c.963C>G
|
ENSP00000343273.4:p.Cys321Trp
|
|
ENST00000409689.5:c.819C>G
|
ENSP00000386263.1:p.Cys273Trp
|
|
ENST00000521082.5:c.*971C>G
|
ENSP00000430351.1:n.*971C>G
|
|
NM_001031710.2:c.963C>G
|
NP_001026880.2:p.Cys321Trp
|
|
NM_018846.4:c.819C>G
|
NP_061334.4:p.Cys273Trp
|
|
NR_033328.1:n.1387C>G
|
|
|
XM_006715753.1:c.1002C>G
|
XP_006715816.1:p.Cys334Trp
|
|
XM_006715754.1:c.936C>G
|
XP_006715817.1:p.Cys312Trp
|
|
XM_006715755.1:c.936C>G
|
XP_006715818.1:p.Cys312Trp
|
|
XM_006715756.1:c.858C>G
|
XP_006715819.1:p.Cys286Trp
|
|
XM_006715753.3:c.1002C>G
|
XP_006715816.1:p.Cys334Trp
|
|
XM_006715754.3:c.936C>G
|
XP_006715817.1:p.Cys312Trp
|
|
XM_006715755.3:c.936C>G
|
XP_006715818.1:p.Cys312Trp
|
|
XM_006715756.3:c.858C>G
|
XP_006715819.1:p.Cys286Trp
|
|
XM_017012439.2:c.897C>G
|
XP_016867928.1:p.Cys299Trp
|
|
NM_001031710.3:c.963C>G
MANE Select
|
NP_001026880.2:p.Cys321Trp
|
|
NM_018846.5:c.819C>G
|
NP_061334.4:p.Cys273Trp
|
|
NR_033328.2:n.1336C>G
|
|
|