ENST00000381733.9:c.766A>T
|
ENSP00000371152.4:p.Ile256Phe
|
|
ENST00000517409.2:n.686A>T
|
|
|
ENST00000518746.2:n.2404A>T
|
|
|
ENST00000519545.6:n.735A>T
|
|
|
ENST00000520781.6:c.643A>T
|
ENSP00000427751.1:p.Ile215Phe
|
|
ENST00000521542.2:n.26A>T
|
|
|
ENST00000635756.1:c.131A>T
|
|
|
ENST00000635944.1:c.*554A>T
|
ENSP00000490195.1:n.*554A>T
|
|
ENST00000635998.1:c.718A>T
|
ENSP00000490506.1:p.Ile240Phe
|
|
ENST00000636009.1:c.575A>T
|
ENSP00000489988.1:n.575A>T
|
|
ENST00000636033.1:c.*554A>T
|
ENSP00000489617.1:n.*554A>T
|
|
ENST00000636050.1:c.*561A>T
|
ENSP00000490562.1:n.*561A>T
|
|
ENST00000636128.1:c.397A>T
|
ENSP00000489789.1:p.Ile133Phe
|
|
ENST00000636160.1:c.*610A>T
|
ENSP00000489651.1:n.*610A>T
|
|
ENST00000636171.1:c.661A>T
|
ENSP00000489761.1:p.Ile221Phe
|
|
ENST00000636455.1:c.766A>T
|
ENSP00000490502.1:p.Ile256Phe
|
|
ENST00000636494.1:c.*498A>T
|
ENSP00000490388.1:n.*498A>T
|
|
ENST00000636563.1:n.380A>T
|
|
|
ENST00000636577.1:c.658A>T
|
ENSP00000490027.1:p.Ile220Phe
|
|
ENST00000636691.1:c.523A>T
|
ENSP00000490725.1:p.Ile175Phe
|
|
ENST00000636701.1:c.*369A>T
|
ENSP00000489800.1:n.*369A>T
|
|
ENST00000636815.1:c.635A>T
|
|
|
ENST00000636920.1:c.*554A>T
|
ENSP00000490437.1:n.*554A>T
|
|
ENST00000636997.1:c.631A>T
|
ENSP00000490093.1:p.Ile211Phe
|
|
ENST00000637013.1:c.*1086A>T
|
ENSP00000490596.1:n.*1086A>T
|
|
ENST00000637014.1:n.1125A>T
|
|
|
ENST00000637095.1:c.*498A>T
|
ENSP00000490415.1:n.*498A>T
|
|
ENST00000637244.1:c.*1236A>T
|
ENSP00000490188.1:n.*1236A>T
|
|
ENST00000637343.1:n.2155A>T
|
|
|
ENST00000637429.1:c.*930A>T
|
ENSP00000490522.1:n.*930A>T
|
|
ENST00000637484.1:c.*680A>T
|
ENSP00000490837.1:n.*680A>T
|
|
ENST00000637528.1:c.655A>T
|
ENSP00000490801.1:p.Ile219Phe
|
|
ENST00000637609.1:n.3439A>T
|
|
|
ENST00000637636.1:c.712A>T
|
ENSP00000490112.1:p.Ile238Phe
|
|
ENST00000637790.2:c.718A>T
MANE Select
|
ENSP00000490272.1:p.Ile240Phe
|
|
ENST00000637857.1:n.1084A>T
|
|
|
ENST00000637922.1:c.523A>T
|
ENSP00000490071.1:p.Ile175Phe
|
|
ENST00000637991.1:c.691A>T
|
ENSP00000489901.1:p.Ile231Phe
|
|
ENST00000638028.1:n.935A>T
|
|
|
ENST00000638069.1:n.1539A>T
|
|
|
ENST00000262097.10:c.718A>T
|
ENSP00000262097.6:p.Ile240Phe
|
|
ENST00000314146.10:c.700A>T
|
ENSP00000326970.10:p.Ile234Phe
|
|
ENST00000381733.8:c.766A>T
|
ENSP00000371152.4:p.Ile256Phe
|
|
ENST00000518746.1:n.535A>T
|
|
|
ENST00000519468.5:n.547A>T
|
|
|
ENST00000520781.5:c.643A>T
|
ENSP00000427751.1:p.Ile215Phe
|
|
ENST00000521542.1:n.431A>T
|
|
|
NM_001127505.1:c.700A>T
|
NP_001120977.1:p.Ile234Phe
|
|
NM_001127505.2:c.700A>T
|
NP_001120977.1:p.Ile234Phe
|
|
NM_004315.4:c.766A>T
|
NP_004306.3:p.Ile256Phe
|
|
NM_004315.5:c.766A>T
|
NP_004306.3:p.Ile256Phe
|
|
NM_177924.3:c.718A>T
|
NP_808592.2:p.Ile240Phe
|
|
NM_177924.4:c.718A>T
|
NP_808592.2:p.Ile240Phe
|
|
XM_005273504.2:c.652A>T
|
XP_005273561.1:p.Ile218Phe
|
|
NM_001363743.1:c.523A>T
|
NP_001350672.1:p.Ile175Phe
|
|
XM_005273504.3:c.652A>T
|
XP_005273561.1:p.Ile218Phe
|
|
NM_177924.5:c.718A>T
MANE Select
|
NP_808592.2:p.Ile240Phe
|
|
NM_001127505.3:c.700A>T
|
NP_001120977.1:p.Ile234Phe
|
|
NM_001363743.2:c.523A>T
|
NP_001350672.1:p.Ile175Phe
|
|
NM_004315.6:c.766A>T
|
NP_004306.3:p.Ile256Phe
|
|