|
ENST00000423275.6:c.*587C>T
|
ENSP00000401088.1:n.*587C>T
|
|
|
ENST00000432427.3:c.242C>T
|
|
|
|
ENST00000465826.6:n.513C>T
|
|
|
|
ENST00000491290.2:n.1299C>T
|
|
|
|
ENST00000684903.1:c.*599C>T
|
ENSP00000508612.1:n.*599C>T
|
|
|
ENST00000685348.1:c.*599C>T
|
ENSP00000510285.1:n.*599C>T
|
|
|
ENST00000685437.1:c.823C>T
|
ENSP00000508794.1:p.Pro275Ser
|
|
|
ENST00000685438.1:n.686C>T
|
|
|
|
ENST00000685653.1:c.922C>T
|
ENSP00000509968.1:p.Pro308Ser
|
|
|
ENST00000685738.1:c.922C>T
|
ENSP00000510156.1:p.Pro308Ser
|
|
|
ENST00000686409.1:n.1630C>T
|
|
|
|
ENST00000686455.1:n.1285C>T
|
|
|
|
ENST00000686479.1:n.1293C>T
|
|
|
|
ENST00000686762.1:c.922C>T
|
ENSP00000509767.1:p.Pro308Ser
|
|
|
ENST00000687257.1:n.1158C>T
|
|
|
|
ENST00000687326.1:c.922C>T
|
ENSP00000509665.1:p.Pro308Ser
|
|
|
ENST00000687486.1:c.182+168C>T
|
|
|
|
ENST00000687505.1:n.1040C>T
|
|
|
|
ENST00000687923.1:c.823C>T
|
ENSP00000510255.1:p.Pro275Ser
|
|
|
ENST00000687940.1:n.1299C>T
|
|
|
|
ENST00000688269.1:n.1518C>T
|
|
|
|
ENST00000688326.1:c.242C>T
|
|
|
|
ENST00000688444.1:n.1248C>T
|
|
|
|
ENST00000688543.1:c.823C>T
|
ENSP00000509612.1:p.Pro275Ser
|
|
|
ENST00000688625.1:c.*500C>T
|
ENSP00000509522.1:n.*500C>T
|
|
|
ENST00000688803.1:n.1153C>T
|
|
|
|
ENST00000689097.1:c.*599C>T
|
ENSP00000509756.1:n.*599C>T
|
|
|
ENST00000689389.1:c.922C>T
|
ENSP00000510213.1:p.Pro308Ser
|
|
|
ENST00000689418.1:c.*599C>T
|
ENSP00000509467.1:n.*599C>T
|
|
|
ENST00000689481.1:c.*599C>T
|
ENSP00000510248.1:n.*599C>T
|
|
|
ENST00000689540.1:n.1072C>T
|
|
|
|
ENST00000689876.1:c.922C>T
|
ENSP00000508535.1:p.Pro308Ser
|
|
|
ENST00000689914.1:c.922C>T
|
ENSP00000509847.1:p.Pro308Ser
|
|
|
ENST00000690397.1:c.811C>T
|
ENSP00000508730.1:p.Pro271Ser
|
|
|
ENST00000690460.1:c.910C>T
|
ENSP00000509106.1:p.Pro304Ser
|
|
|
ENST00000690625.1:n.1225C>T
|
|
|
|
ENST00000691268.1:c.349C>T
|
|
|
|
ENST00000691396.1:c.*715C>T
|
ENSP00000510712.1:n.*715C>T
|
|
|
ENST00000691724.1:c.922C>T
|
ENSP00000509255.1:p.Pro308Ser
|
|
|
ENST00000691779.1:c.*500C>T
|
ENSP00000508592.1:n.*500C>T
|
|
|
ENST00000691899.1:c.922C>T
|
ENSP00000508763.1:p.Pro308Ser
|
|
|
ENST00000692069.1:n.1145C>T
|
|
|
|
ENST00000692093.1:c.823C>T
|
ENSP00000509669.1:p.Pro275Ser
|
|
|
ENST00000692311.1:n.1403C>T
|
|
|
|
ENST00000692558.1:n.1287C>T
|
|
|
|
ENST00000692773.1:c.*659C>T
|
ENSP00000509055.1:n.*659C>T
|
|
|
ENST00000692830.1:c.*667C>T
|
ENSP00000509461.1:n.*667C>T
|
|
|
ENST00000693069.1:c.823C>T
|
ENSP00000510072.1:p.Pro275Ser
|
|
|
ENST00000693312.1:c.697C>T
|
ENSP00000508686.1:p.Pro233Ser
|
|
|
ENST00000693664.1:c.922C>T
|
ENSP00000509614.1:p.Pro308Ser
|
|
|
ENST00000693705.1:c.*599C>T
|
ENSP00000510697.1:n.*599C>T
|
|
|
ENST00000251849.9:c.922C>T
MANE Select
|
ENSP00000251849.4:p.Pro308Ser
|
|
|
ENST00000442415.7:c.982C>T
|
ENSP00000401888.2:p.Pro328Ser
|
|
|
ENST00000251849.8:c.922C>T
|
ENSP00000251849.4:p.Pro308Ser
|
|
|
ENST00000423275.5:c.*599C>T
|
ENSP00000401088.1:n.*599C>T
|
|
|
ENST00000432427.2:c.559C>T
|
ENSP00000398591.2:p.Pro187Ser
|
|
|
ENST00000442415.6:c.982C>T
|
ENSP00000401888.2:p.Pro328Ser
|
|
|
ENST00000465826.5:n.166C>T
|
|
|
|
ENST00000491290.1:n.551C>T
|
|
|
|
NM_002880.3:c.922C>T , LRG_413t1:c.922C>T
|
NP_002871.1:p.Pro308Ser
|
|
|
XM_005265355.1:c.922C>T
|
XP_005265412.1:p.Pro308Ser
|
|
|
XM_005265357.1:c.823C>T
|
XP_005265414.1:p.Pro275Ser
|
|
|
XM_005265358.3:c.679C>T
|
XP_005265415.1:p.Pro227Ser
|
|
|
XM_005265359.3:c.580C>T
|
XP_005265416.1:p.Pro194Ser
|
|
|
XM_005265360.1:c.922C>T
|
XP_005265417.1:p.Pro308Ser
|
|
|
XM_011533974.1:c.922C>T
|
XP_011532276.1:p.Pro308Ser
|
|
|
XM_011533975.1:c.679C>T
|
XP_011532277.1:p.Pro227Ser
|
|
|
NM_001354689.1:c.982C>T
|
NP_001341618.1:p.Pro328Ser
|
|
|
NM_001354690.1:c.922C>T
|
NP_001341619.1:p.Pro308Ser
|
|
|
NM_001354691.1:c.679C>T
|
NP_001341620.1:p.Pro227Ser
|
|
|
NM_001354692.1:c.679C>T
|
NP_001341621.1:p.Pro227Ser
|
|
|
NM_001354693.1:c.823C>T
|
NP_001341622.1:p.Pro275Ser
|
|
|
NM_001354694.1:c.739C>T
|
NP_001341623.1:p.Pro247Ser
|
|
|
NM_001354695.1:c.580C>T
|
NP_001341624.1:p.Pro194Ser
|
|
|
NR_148940.1:n.1337C>T
|
|
|
|
NR_148941.1:n.1337C>T
|
|
|
|
NR_148942.1:n.1337C>T
|
|
|
|
XM_011533974.3:c.922C>T
|
XP_011532276.1:p.Pro308Ser
|
|
|
XM_017006966.1:c.823C>T
|
XP_016862455.1:p.Pro275Ser
|
|
|
XR_001740227.1:n.1154C>T
|
|
|
|
NM_001354689.3:c.982C>T
|
NP_001341618.1:p.Pro328Ser
|
|
|
NM_001354690.2:c.922C>T
|
NP_001341619.1:p.Pro308Ser
|
|
|
NM_001354691.2:c.679C>T
|
NP_001341620.1:p.Pro227Ser
|
|
|
NM_001354692.2:c.679C>T
|
NP_001341621.1:p.Pro227Ser
|
|
|
NM_001354693.2:c.823C>T
|
NP_001341622.1:p.Pro275Ser
|
|
|
NM_001354694.2:c.739C>T
|
NP_001341623.1:p.Pro247Ser
|
|
|
NM_001354695.2:c.580C>T
|
NP_001341624.1:p.Pro194Ser
|
|
|
NR_148940.2:n.1253C>T
|
|
|
|
NR_148941.2:n.1253C>T
|
|
|
|
NR_148942.2:n.1253C>T
|
|
|
|
NM_001354690.3:c.922C>T
|
NP_001341619.1:p.Pro308Ser
|
|
|
NM_001354691.3:c.679C>T
|
NP_001341620.1:p.Pro227Ser
|
|
|
NM_001354692.3:c.679C>T
|
NP_001341621.1:p.Pro227Ser
|
|
|
NM_001354693.3:c.823C>T
|
NP_001341622.1:p.Pro275Ser
|
|
|
NM_001354694.3:c.739C>T
|
NP_001341623.1:p.Pro247Ser
|
|
|
NM_001354695.3:c.580C>T
|
NP_001341624.1:p.Pro194Ser
|
|
|
NM_002880.4:c.922C>T
MANE Select
|
NP_002871.1:p.Pro308Ser
|
|
|
NR_148940.3:n.1253C>T
|
|
|
|
NR_148941.3:n.1253C>T
|
|
|
|
NR_148942.3:n.1253C>T
|
|
|
