|
ENST00000423275.6:c.*734T>G
|
ENSP00000401088.1:n.*734T>G
|
|
|
ENST00000432427.3:c.389T>G
|
|
|
|
ENST00000465826.6:n.660T>G
|
|
|
|
ENST00000491290.2:n.1446T>G
|
|
|
|
ENST00000684903.1:c.*746T>G
|
ENSP00000508612.1:n.*746T>G
|
|
|
ENST00000685348.1:c.*746T>G
|
ENSP00000510285.1:n.*746T>G
|
|
|
ENST00000685437.1:c.970T>G
|
ENSP00000508794.1:p.Ser324Ala
|
|
|
ENST00000685653.1:c.1069T>G
|
ENSP00000509968.1:p.Ser357Ala
|
|
|
ENST00000685738.1:c.1069T>G
|
ENSP00000510156.1:p.Ser357Ala
|
|
|
ENST00000686409.1:n.2120T>G
|
|
|
|
ENST00000686455.1:n.1432T>G
|
|
|
|
ENST00000686479.1:n.1440T>G
|
|
|
|
ENST00000686762.1:c.1069T>G
|
ENSP00000509767.1:p.Ser357Ala
|
|
|
ENST00000687257.1:n.1305T>G
|
|
|
|
ENST00000687326.1:c.1069T>G
|
ENSP00000509665.1:p.Ser357Ala
|
|
|
ENST00000687486.1:c.261T>G
|
|
|
|
ENST00000687505.1:n.1187T>G
|
|
|
|
ENST00000687923.1:c.970T>G
|
ENSP00000510255.1:p.Ser324Ala
|
|
|
ENST00000687940.1:n.1446T>G
|
|
|
|
ENST00000688269.1:n.1665T>G
|
|
|
|
ENST00000688326.1:c.389T>G
|
|
|
|
ENST00000688444.1:n.1395T>G
|
|
|
|
ENST00000688543.1:c.970T>G
|
ENSP00000509612.1:p.Ser324Ala
|
|
|
ENST00000688625.1:c.*647T>G
|
ENSP00000509522.1:n.*647T>G
|
|
|
ENST00000688803.1:n.1300T>G
|
|
|
|
ENST00000688914.1:n.55T>G
|
|
|
|
ENST00000689097.1:c.*746T>G
|
ENSP00000509756.1:n.*746T>G
|
|
|
ENST00000689389.1:c.1069T>G
|
ENSP00000510213.1:p.Ser357Ala
|
|
|
ENST00000689418.1:c.*746T>G
|
ENSP00000509467.1:n.*746T>G
|
|
|
ENST00000689481.1:c.*746T>G
|
ENSP00000510248.1:n.*746T>G
|
|
|
ENST00000689540.1:n.1219T>G
|
|
|
|
ENST00000689876.1:c.1069T>G
|
ENSP00000508535.1:p.Ser357Ala
|
|
|
ENST00000689914.1:c.1069T>G
|
ENSP00000509847.1:p.Ser357Ala
|
|
|
ENST00000690397.1:c.958T>G
|
ENSP00000508730.1:p.Ser320Ala
|
|
|
ENST00000690460.1:c.1057T>G
|
ENSP00000509106.1:p.Ser353Ala
|
|
|
ENST00000690625.1:n.1372T>G
|
|
|
|
ENST00000691268.1:c.496T>G
|
|
|
|
ENST00000691396.1:c.*862T>G
|
ENSP00000510712.1:n.*862T>G
|
|
|
ENST00000691724.1:c.*26T>G
|
ENSP00000509255.1:n.*26T>G
|
|
|
ENST00000691779.1:c.*647T>G
|
ENSP00000508592.1:n.*647T>G
|
|
|
ENST00000691899.1:c.1069T>G
|
ENSP00000508763.1:p.Ser357Ala
|
|
|
ENST00000692069.1:n.1635T>G
|
|
|
|
ENST00000692093.1:c.970T>G
|
ENSP00000509669.1:p.Ser324Ala
|
|
|
ENST00000692311.1:n.1893T>G
|
|
|
|
ENST00000692558.1:n.1434T>G
|
|
|
|
ENST00000692773.1:c.*806T>G
|
ENSP00000509055.1:n.*806T>G
|
|
|
ENST00000692830.1:c.*814T>G
|
ENSP00000509461.1:n.*814T>G
|
|
|
ENST00000693069.1:c.970T>G
|
ENSP00000510072.1:p.Ser324Ala
|
|
|
ENST00000693312.1:c.844T>G
|
ENSP00000508686.1:p.Ser282Ala
|
|
|
ENST00000693664.1:c.1069T>G
|
ENSP00000509614.1:p.Ser357Ala
|
|
|
ENST00000693705.1:c.*746T>G
|
ENSP00000510697.1:n.*746T>G
|
|
|
ENST00000251849.9:c.1069T>G
MANE Select
|
ENSP00000251849.4:p.Ser357Ala
|
|
|
ENST00000442415.7:c.1129T>G
|
ENSP00000401888.2:p.Ser377Ala
|
|
|
ENST00000251849.8:c.1069T>G
|
ENSP00000251849.4:p.Ser357Ala
|
|
|
ENST00000423275.5:c.*746T>G
|
ENSP00000401088.1:n.*746T>G
|
|
|
ENST00000432427.2:c.706T>G
|
ENSP00000398591.2:p.Ser236Ala
|
|
|
ENST00000442415.6:c.1129T>G
|
ENSP00000401888.2:p.Ser377Ala
|
|
|
ENST00000460610.1:n.26T>G
|
|
|
|
ENST00000465826.5:n.313T>G
|
|
|
|
NM_002880.3:c.1069T>G , LRG_413t1:c.1069T>G
|
NP_002871.1:p.Ser357Ala
|
|
|
XM_005265355.1:c.1069T>G
|
XP_005265412.1:p.Ser357Ala
|
|
|
XM_005265357.1:c.970T>G
|
XP_005265414.1:p.Ser324Ala
|
|
|
XM_005265358.3:c.826T>G
|
XP_005265415.1:p.Ser276Ala
|
|
|
XM_005265359.3:c.727T>G
|
XP_005265416.1:p.Ser243Ala
|
|
|
XM_005265360.1:c.1069T>G
|
XP_005265417.1:p.Ser357Ala
|
|
|
XM_011533974.1:c.1069T>G
|
XP_011532276.1:p.Ser357Ala
|
|
|
XM_011533975.1:c.826T>G
|
XP_011532277.1:p.Ser276Ala
|
|
|
NM_001354689.1:c.1129T>G
|
NP_001341618.1:p.Ser377Ala
|
|
|
NM_001354690.1:c.1069T>G
|
NP_001341619.1:p.Ser357Ala
|
|
|
NM_001354691.1:c.826T>G
|
NP_001341620.1:p.Ser276Ala
|
|
|
NM_001354692.1:c.826T>G
|
NP_001341621.1:p.Ser276Ala
|
|
|
NM_001354693.1:c.970T>G
|
NP_001341622.1:p.Ser324Ala
|
|
|
NM_001354694.1:c.886T>G
|
NP_001341623.1:p.Ser296Ala
|
|
|
NM_001354695.1:c.727T>G
|
NP_001341624.1:p.Ser243Ala
|
|
|
NR_148940.1:n.1484T>G
|
|
|
|
NR_148941.1:n.1484T>G
|
|
|
|
NR_148942.1:n.1482T>G
|
|
|
|
XM_011533974.3:c.1069T>G
|
XP_011532276.1:p.Ser357Ala
|
|
|
XM_017006966.1:c.970T>G
|
XP_016862455.1:p.Ser324Ala
|
|
|
XR_001740227.1:n.1301T>G
|
|
|
|
NM_001354689.3:c.1129T>G
|
NP_001341618.1:p.Ser377Ala
|
|
|
NM_001354690.2:c.1069T>G
|
NP_001341619.1:p.Ser357Ala
|
|
|
NM_001354691.2:c.826T>G
|
NP_001341620.1:p.Ser276Ala
|
|
|
NM_001354692.2:c.826T>G
|
NP_001341621.1:p.Ser276Ala
|
|
|
NM_001354693.2:c.970T>G
|
NP_001341622.1:p.Ser324Ala
|
|
|
NM_001354694.2:c.886T>G
|
NP_001341623.1:p.Ser296Ala
|
|
|
NM_001354695.2:c.727T>G
|
NP_001341624.1:p.Ser243Ala
|
|
|
NR_148940.2:n.1400T>G
|
|
|
|
NR_148941.2:n.1400T>G
|
|
|
|
NR_148942.2:n.1398T>G
|
|
|
|
NM_001354690.3:c.1069T>G
|
NP_001341619.1:p.Ser357Ala
|
|
|
NM_001354691.3:c.826T>G
|
NP_001341620.1:p.Ser276Ala
|
|
|
NM_001354692.3:c.826T>G
|
NP_001341621.1:p.Ser276Ala
|
|
|
NM_001354693.3:c.970T>G
|
NP_001341622.1:p.Ser324Ala
|
|
|
NM_001354694.3:c.886T>G
|
NP_001341623.1:p.Ser296Ala
|
|
|
NM_001354695.3:c.727T>G
|
NP_001341624.1:p.Ser243Ala
|
|
|
NM_002880.4:c.1069T>G
MANE Select
|
NP_002871.1:p.Ser357Ala
|
|
|
NR_148940.3:n.1400T>G
|
|
|
|
NR_148941.3:n.1400T>G
|
|
|
|
NR_148942.3:n.1398T>G
|
|
|
