|
ENST00000711048.1:c.*153C>G
|
ENSP00000518557.1:n.*153C>G
|
|
|
ENST00000402731.6:c.1217C>G
|
ENSP00000384835.2:p.Ala406Gly
|
|
|
ENST00000404276.6:c.1418C>G
MANE Select
|
ENSP00000385747.1:p.Ala473Gly
|
|
|
ENST00000425190.7:c.755C>G
|
ENSP00000390244.2:p.Ala252Gly
|
|
|
ENST00000464581.6:c.758C>G
|
ENSP00000483777.2:p.Ala253Gly
|
|
|
ENST00000648295.1:n.970C>G
|
|
|
|
ENST00000649563.1:c.755C>G
|
ENSP00000496928.1:p.Ala252Gly
|
|
|
ENST00000650281.1:c.1418C>G
|
ENSP00000497000.1:p.Ala473Gly
|
|
|
ENST00000328354.10:c.1418C>G
|
ENSP00000329178.6:p.Ala473Gly
|
|
|
ENST00000348295.7:c.1331C>G
|
ENSP00000329012.5:p.Ala444Gly
|
|
|
ENST00000382580.6:c.1547C>G
|
ENSP00000372023.2:p.Ala516Gly
|
|
|
ENST00000402731.5:c.1331C>G
|
ENSP00000384835.1:p.Ala444Gly
|
|
|
ENST00000403642.5:c.1145C>G
|
ENSP00000384919.1:p.Ala382Gly
|
|
|
ENST00000404276.5:c.1418C>G
|
ENSP00000385747.1:p.Ala473Gly
|
|
|
ENST00000405598.5:c.1418C>G
|
ENSP00000386087.1:p.Ala473Gly
|
|
|
ENST00000416671.5:c.*908C>G
|
ENSP00000402225.1:n.*908C>G
|
|
|
ENST00000417588.5:c.1327C>G
|
ENSP00000412901.1:n.1327C>G
|
|
|
ENST00000433728.5:c.1356C>G
|
ENSP00000404400.1:n.1356C>G
|
|
|
ENST00000434810.5:c.616C>G
|
|
|
|
ENST00000448511.5:c.1308C>G
|
ENSP00000404567.1:n.1308C>G
|
|
|
ENST00000456369.5:c.264-4860C>G
|
|
|
|
NM_001005735.1:c.1547C>G
|
NP_001005735.1:p.Ala516Gly
|
|
|
NM_001257387.1:c.755C>G
|
NP_001244316.1:p.Ala252Gly
|
|
|
NM_007194.3:c.1418C>G
|
NP_009125.1:p.Ala473Gly
|
|
|
NM_145862.2:c.1331C>G
|
NP_665861.1:p.Ala444Gly
|
|
|
XM_006724114.2:c.938C>G
|
XP_006724177.1:p.Ala313Gly
|
|
|
XM_006724116.2:c.875C>G
|
XP_006724179.2:p.Ala292Gly
|
|
|
XM_011529839.1:c.1577C>G
|
XP_011528141.1:p.Ala526Gly
|
|
|
XM_011529840.1:c.1490C>G
|
XP_011528142.1:p.Ala497Gly
|
|
|
XM_011529841.1:c.1346C>G
|
XP_011528143.1:p.Ala449Gly
|
|
|
XM_011529842.1:c.1247C>G
|
XP_011528144.1:p.Ala416Gly
|
|
|
XM_011529843.1:c.1217C>G
|
XP_011528145.1:p.Ala406Gly
|
|
|
XM_011529845.1:c.755C>G
|
XP_011528147.1:p.Ala252Gly
|
|
|
XR_937805.1:n.1577C>G
|
|
|
|
NM_001349956.1:c.1217C>G
|
NP_001336885.1:p.Ala406Gly
|
|
|
NM_007194.4:c.1418C>G
MANE Select
|
NP_009125.1:p.Ala473Gly
|
|
|
XM_006724114.3:c.971C>G
|
XP_006724177.2:p.Ala324Gly
|
|
|
XM_011529839.2:c.1577C>G
|
XP_011528141.1:p.Ala526Gly
|
|
|
XM_011529840.3:c.1490C>G
|
XP_011528142.1:p.Ala497Gly
|
|
|
XM_011529842.2:c.1247C>G
|
XP_011528144.1:p.Ala416Gly
|
|
|
XM_011529845.2:c.755C>G
|
XP_011528147.1:p.Ala252Gly
|
|
|
XM_017028560.1:c.1541C>G
|
XP_016884049.1:p.Ala514Gly
|
|
|
XM_017028561.2:c.755C>G
|
XP_016884050.1:p.Ala252Gly
|
|
|
XM_024452148.1:c.1448C>G
|
XP_024307916.1:p.Ala483Gly
|
|
|
XM_024452149.1:c.1361C>G
|
XP_024307917.1:p.Ala454Gly
|
|
|
XR_937805.2:n.1588C>G
|
|
|
|
NM_001005735.2:c.1547C>G
|
NP_001005735.1:p.Ala516Gly
|
|
|
NM_001257387.2:c.755C>G
|
NP_001244316.1:p.Ala252Gly
|
|
|
NM_001349956.2:c.1217C>G
|
NP_001336885.1:p.Ala406Gly
|
|
