ENST00000381733.9:c.782A>T
|
ENSP00000371152.4:p.Asp261Val
|
|
ENST00000517409.2:n.702A>T
|
|
|
ENST00000518746.2:n.2420A>T
|
|
|
ENST00000519545.6:n.751A>T
|
|
|
ENST00000520781.6:c.659A>T
|
ENSP00000427751.1:p.Asp220Val
|
|
ENST00000521542.2:n.42A>T
|
|
|
ENST00000635756.1:c.147A>T
|
|
|
ENST00000635944.1:c.*570A>T
|
ENSP00000490195.1:n.*570A>T
|
|
ENST00000635998.1:c.734A>T
|
ENSP00000490506.1:p.Asp245Val
|
|
ENST00000636009.1:c.591A>T
|
ENSP00000489988.1:n.591A>T
|
|
ENST00000636033.1:c.*570A>T
|
ENSP00000489617.1:n.*570A>T
|
|
ENST00000636050.1:c.*577A>T
|
ENSP00000490562.1:n.*577A>T
|
|
ENST00000636128.1:c.413A>T
|
ENSP00000489789.1:p.Asp138Val
|
|
ENST00000636160.1:c.*626A>T
|
ENSP00000489651.1:n.*626A>T
|
|
ENST00000636171.1:c.677A>T
|
ENSP00000489761.1:p.Asp226Val
|
|
ENST00000636455.1:c.782A>T
|
ENSP00000490502.1:p.Asp261Val
|
|
ENST00000636494.1:c.*514A>T
|
ENSP00000490388.1:n.*514A>T
|
|
ENST00000636563.1:n.396A>T
|
|
|
ENST00000636577.1:c.674A>T
|
ENSP00000490027.1:p.Asp225Val
|
|
ENST00000636691.1:c.539A>T
|
ENSP00000490725.1:p.Asp180Val
|
|
ENST00000636701.1:c.*385A>T
|
ENSP00000489800.1:n.*385A>T
|
|
ENST00000636815.1:c.651A>T
|
|
|
ENST00000636920.1:c.*570A>T
|
ENSP00000490437.1:n.*570A>T
|
|
ENST00000636997.1:c.647A>T
|
ENSP00000490093.1:p.Asp216Val
|
|
ENST00000637013.1:c.*1102A>T
|
ENSP00000490596.1:n.*1102A>T
|
|
ENST00000637014.1:n.1141A>T
|
|
|
ENST00000637095.1:c.*514A>T
|
ENSP00000490415.1:n.*514A>T
|
|
ENST00000637244.1:c.*1252A>T
|
ENSP00000490188.1:n.*1252A>T
|
|
ENST00000637343.1:n.2171A>T
|
|
|
ENST00000637429.1:c.*946A>T
|
ENSP00000490522.1:n.*946A>T
|
|
ENST00000637484.1:c.*696A>T
|
ENSP00000490837.1:n.*696A>T
|
|
ENST00000637528.1:c.671A>T
|
ENSP00000490801.1:p.Asp224Val
|
|
ENST00000637609.1:n.3455A>T
|
|
|
ENST00000637636.1:c.728A>T
|
ENSP00000490112.1:p.Asp243Val
|
|
ENST00000637790.2:c.734A>T
MANE Select
|
ENSP00000490272.1:p.Asp245Val
|
|
ENST00000637857.1:n.1100A>T
|
|
|
ENST00000637922.1:c.539A>T
|
ENSP00000490071.1:p.Asp180Val
|
|
ENST00000637991.1:c.707A>T
|
ENSP00000489901.1:p.Asp236Val
|
|
ENST00000638028.1:n.951A>T
|
|
|
ENST00000638069.1:n.1555A>T
|
|
|
ENST00000262097.10:c.734A>T
|
ENSP00000262097.6:p.Asp245Val
|
|
ENST00000314146.10:c.716A>T
|
ENSP00000326970.10:p.Asp239Val
|
|
ENST00000381733.8:c.782A>T
|
ENSP00000371152.4:p.Asp261Val
|
|
ENST00000518746.1:n.551A>T
|
|
|
ENST00000519468.5:n.563A>T
|
|
|
ENST00000520781.5:c.659A>T
|
ENSP00000427751.1:p.Asp220Val
|
|
ENST00000521542.1:n.447A>T
|
|
|
NM_001127505.1:c.716A>T
|
NP_001120977.1:p.Asp239Val
|
|
NM_001127505.2:c.716A>T
|
NP_001120977.1:p.Asp239Val
|
|
NM_004315.4:c.782A>T
|
NP_004306.3:p.Asp261Val
|
|
NM_004315.5:c.782A>T
|
NP_004306.3:p.Asp261Val
|
|
NM_177924.3:c.734A>T
|
NP_808592.2:p.Asp245Val
|
|
NM_177924.4:c.734A>T
|
NP_808592.2:p.Asp245Val
|
|
XM_005273504.2:c.668A>T
|
XP_005273561.1:p.Asp223Val
|
|
NM_001363743.1:c.539A>T
|
NP_001350672.1:p.Asp180Val
|
|
XM_005273504.3:c.668A>T
|
XP_005273561.1:p.Asp223Val
|
|
NM_177924.5:c.734A>T
MANE Select
|
NP_808592.2:p.Asp245Val
|
|
NM_001127505.3:c.716A>T
|
NP_001120977.1:p.Asp239Val
|
|
NM_001363743.2:c.539A>T
|
NP_001350672.1:p.Asp180Val
|
|
NM_004315.6:c.782A>T
|
NP_004306.3:p.Asp261Val
|
|