|
ENST00000482632.6:n.1664A>T
|
|
|
|
ENST00000686600.1:c.1254A>T
|
ENSP00000509268.1:p.Gln418His
|
|
|
ENST00000686799.1:n.1351A>T
|
|
|
|
ENST00000687427.1:c.1254A>T
|
ENSP00000509426.1:p.Gln418His
|
|
|
ENST00000687817.1:c.*1401A>T
|
ENSP00000508926.1:n.*1401A>T
|
|
|
ENST00000687972.1:c.1314A>T
|
ENSP00000509208.1:p.Gln438His
|
|
|
ENST00000689261.1:n.1161A>T
|
|
|
|
ENST00000689401.1:c.*1504A>T
|
ENSP00000510251.1:n.*1504A>T
|
|
|
ENST00000689423.1:c.*1504A>T
|
ENSP00000508519.1:n.*1504A>T
|
|
|
ENST00000690095.1:n.1642A>T
|
|
|
|
ENST00000690139.1:c.*955A>T
|
ENSP00000510483.1:n.*955A>T
|
|
|
ENST00000692458.1:n.1621A>T
|
|
|
|
ENST00000693147.1:c.*1270A>T
|
ENSP00000510358.1:n.*1270A>T
|
|
|
ENST00000262554.7:c.1254A>T
MANE Select
|
ENSP00000262554.2:p.Gln418His
|
|
|
ENST00000642671.1:c.1555A>T
|
ENSP00000495764.1:n.1555A>T
|
|
|
ENST00000643599.1:c.1322A>T
|
ENSP00000494770.1:n.1322A>T
|
|
|
ENST00000644140.1:c.*995A>T
|
ENSP00000493933.1:n.*995A>T
|
|
|
ENST00000646481.1:c.1186A>T
|
ENSP00000496627.1:n.1186A>T
|
|
|
ENST00000646534.1:c.*1057A>T
|
ENSP00000495388.1:n.*1057A>T
|
|
|
ENST00000262554.6:c.1254A>T
|
ENSP00000262554.2:p.Gln418His
|
|
|
ENST00000469778.1:n.211A>T
|
|
|
|
NM_001281303.1:c.1254A>T
|
NP_001268232.1:p.Gln418His
|
|
|
NM_006415.3:c.1254A>T
|
NP_006406.1:p.Gln418His
|
|
|
XM_011518139.1:c.789A>T
|
XP_011516441.1:p.Gln263His
|
|
|
XM_011518139.3:c.789A>T
|
XP_011516441.1:p.Gln263His
|
|
|
XM_017014200.2:c.888A>T
|
XP_016869689.1:p.Gln296His
|
|
|
XM_017014201.2:c.888A>T
|
XP_016869690.1:p.Gln296His
|
|
|
XM_024447378.1:c.789A>T
|
XP_024303146.1:p.Gln263His
|
|
|
XM_024447379.1:c.789A>T
|
XP_024303147.1:p.Gln263His
|
|
|
XR_002956744.1:n.1404A>T
|
|
|
|
NM_006415.4:c.1254A>T
MANE Select
|
NP_006406.1:p.Gln418His
|
|
|
NM_001281303.2:c.1254A>T
|
NP_001268232.1:p.Gln418His
|
|
|
NM_001368272.1:c.888A>T
|
NP_001355201.1:p.Gln296His
|
|
|
NM_001368273.1:c.789A>T
|
NP_001355202.1:p.Gln263His
|
|
