ENST00000381733.9:c.789G>C
|
ENSP00000371152.4:p.Met263Ile
|
|
ENST00000517409.2:n.709G>C
|
|
|
ENST00000518746.2:n.2427G>C
|
|
|
ENST00000519545.6:n.758G>C
|
|
|
ENST00000520781.6:c.666G>C
|
ENSP00000427751.1:p.Met222Ile
|
|
ENST00000521542.2:n.49G>C
|
|
|
ENST00000635756.1:c.154G>C
|
|
|
ENST00000635944.1:c.*577G>C
|
ENSP00000490195.1:n.*577G>C
|
|
ENST00000635998.1:c.741G>C
|
ENSP00000490506.1:p.Met247Ile
|
|
ENST00000636009.1:c.598G>C
|
ENSP00000489988.1:n.598G>C
|
|
ENST00000636033.1:c.*577G>C
|
ENSP00000489617.1:n.*577G>C
|
|
ENST00000636050.1:c.*584G>C
|
ENSP00000490562.1:n.*584G>C
|
|
ENST00000636128.1:c.420G>C
|
ENSP00000489789.1:p.Met140Ile
|
|
ENST00000636160.1:c.*633G>C
|
ENSP00000489651.1:n.*633G>C
|
|
ENST00000636171.1:c.684G>C
|
ENSP00000489761.1:p.Met228Ile
|
|
ENST00000636455.1:c.789G>C
|
ENSP00000490502.1:p.Met263Ile
|
|
ENST00000636494.1:c.*521G>C
|
ENSP00000490388.1:n.*521G>C
|
|
ENST00000636563.1:n.403G>C
|
|
|
ENST00000636577.1:c.681G>C
|
ENSP00000490027.1:p.Met227Ile
|
|
ENST00000636691.1:c.546G>C
|
ENSP00000490725.1:p.Met182Ile
|
|
ENST00000636701.1:c.*392G>C
|
ENSP00000489800.1:n.*392G>C
|
|
ENST00000636815.1:c.658G>C
|
|
|
ENST00000636920.1:c.*577G>C
|
ENSP00000490437.1:n.*577G>C
|
|
ENST00000636997.1:c.654G>C
|
ENSP00000490093.1:p.Met218Ile
|
|
ENST00000637013.1:c.*1109G>C
|
ENSP00000490596.1:n.*1109G>C
|
|
ENST00000637014.1:n.1148G>C
|
|
|
ENST00000637095.1:c.*521G>C
|
ENSP00000490415.1:n.*521G>C
|
|
ENST00000637244.1:c.*1259G>C
|
ENSP00000490188.1:n.*1259G>C
|
|
ENST00000637343.1:n.2178G>C
|
|
|
ENST00000637429.1:c.*953G>C
|
ENSP00000490522.1:n.*953G>C
|
|
ENST00000637484.1:c.*703G>C
|
ENSP00000490837.1:n.*703G>C
|
|
ENST00000637528.1:c.678G>C
|
ENSP00000490801.1:p.Met226Ile
|
|
ENST00000637609.1:n.3462G>C
|
|
|
ENST00000637636.1:c.735G>C
|
ENSP00000490112.1:p.Met245Ile
|
|
ENST00000637790.2:c.741G>C
MANE Select
|
ENSP00000490272.1:p.Met247Ile
|
|
ENST00000637857.1:n.1107G>C
|
|
|
ENST00000637922.1:c.546G>C
|
ENSP00000490071.1:p.Met182Ile
|
|
ENST00000637991.1:c.714G>C
|
ENSP00000489901.1:p.Met238Ile
|
|
ENST00000638028.1:n.958G>C
|
|
|
ENST00000638069.1:n.1562G>C
|
|
|
ENST00000262097.10:c.741G>C
|
ENSP00000262097.6:p.Met247Ile
|
|
ENST00000314146.10:c.723G>C
|
ENSP00000326970.10:p.Met241Ile
|
|
ENST00000381733.8:c.789G>C
|
ENSP00000371152.4:p.Met263Ile
|
|
ENST00000518746.1:n.558G>C
|
|
|
ENST00000519468.5:n.570G>C
|
|
|
ENST00000520781.5:c.666G>C
|
ENSP00000427751.1:p.Met222Ile
|
|
ENST00000521542.1:n.454G>C
|
|
|
NM_001127505.1:c.723G>C
|
NP_001120977.1:p.Met241Ile
|
|
NM_001127505.2:c.723G>C
|
NP_001120977.1:p.Met241Ile
|
|
NM_004315.4:c.789G>C
|
NP_004306.3:p.Met263Ile
|
|
NM_004315.5:c.789G>C
|
NP_004306.3:p.Met263Ile
|
|
NM_177924.3:c.741G>C
|
NP_808592.2:p.Met247Ile
|
|
NM_177924.4:c.741G>C
|
NP_808592.2:p.Met247Ile
|
|
XM_005273504.2:c.675G>C
|
XP_005273561.1:p.Met225Ile
|
|
NM_001363743.1:c.546G>C
|
NP_001350672.1:p.Met182Ile
|
|
XM_005273504.3:c.675G>C
|
XP_005273561.1:p.Met225Ile
|
|
NM_177924.5:c.741G>C
MANE Select
|
NP_808592.2:p.Met247Ile
|
|
NM_001127505.3:c.723G>C
|
NP_001120977.1:p.Met241Ile
|
|
NM_001363743.2:c.546G>C
|
NP_001350672.1:p.Met182Ile
|
|
NM_004315.6:c.789G>C
|
NP_004306.3:p.Met263Ile
|
|