|
NM_002184.4:c.2731C>T
MANE Select
|
NP_002175.2:p.Arg911Trp
|
|
ENST00000381298.7:c.2731C>T
MANE Select
|
ENSP00000370698.2:p.Arg911Trp
|
|
NM_001190981.1:c.2548C>T
|
NP_001177910.1:p.Arg850Trp
|
|
NM_001190981.2:c.2548C>T
|
NP_001177910.1:p.Arg850Trp
|
|
NM_001364275.1:c.2629C>T
|
NP_001351204.1:p.Arg877Trp
|
|
NM_001364275.2:c.2629C>T
|
NP_001351204.1:p.Arg877Trp
|
|
NM_001364276.1:c.2521C>T
|
NP_001351205.1:p.Arg841Trp
|
|
NM_001364276.2:c.2521C>T
|
NP_001351205.1:p.Arg841Trp
|
|
NM_001364277.1:c.1864C>T
|
NP_001351206.1:p.Arg622Trp
|
|
NM_001364277.2:c.1864C>T
|
NP_001351206.1:p.Arg622Trp
|
|
NM_001364278.1:c.1828C>T
|
NP_001351207.1:p.Arg610Trp
|
|
NM_001364278.2:c.1828C>T
|
NP_001351207.1:p.Arg610Trp
|
|
NM_001364279.1:c.1735C>T
|
NP_001351208.1:p.Arg579Trp
|
|
NM_001364279.2:c.1735C>T
|
NP_001351208.1:p.Arg579Trp
|
|
NM_002184.3:c.2731C>T
|
NP_002175.2:p.Arg911Trp
|
|
NM_175767.2:c.*1658C>T
|
NP_786943.1:n.*1658C>T
|
|
NM_175767.3:c.*1658C>T
|
NP_786943.1:n.*1658C>T
|
|
NR_120480.1:n.3090C>T
|
|
|
NR_120480.2:n.3060C>T
|
|
|
NR_157112.1:n.3895C>T
|
|
|
NR_157112.2:n.3895C>T
|
|
|
ENST00000336909.9:c.2731C>T
|
ENSP00000338799.5:p.Arg911Trp
|
|
ENST00000381287.8:c.*1658C>T
|
ENSP00000370687.4:n.*1658C>T
|
|
ENST00000381294.7:c.2548C>T
|
ENSP00000370694.3:p.Arg850Trp
|
|
ENST00000381294.8:c.2548C>T
|
ENSP00000370694.3:p.Arg850Trp
|
|
ENST00000381298.6:c.2731C>T
|
ENSP00000370698.2:p.Arg911Trp
|
|
ENST00000502326.7:c.2731C>T
|
ENSP00000462158.1:p.Arg911Trp
|
|
ENST00000503773.6:c.*1775C>T
|
ENSP00000426224.2:n.*1775C>T
|
|
ENST00000506241.2:n.4072C>T
|
|
|
ENST00000577363.2:c.*2136C>T
|
ENSP00000513861.1:n.*2136C>T
|
|
ENST00000651614.1:c.*1683C>T
|
ENSP00000498224.1:n.*1683C>T
|
|
ENST00000698638.1:c.1828C>T
|
ENSP00000513851.1:p.Arg610Trp
|
|
ENST00000698639.1:c.2584C>T
|
ENSP00000513852.1:p.Arg862Trp
|
|
ENST00000698640.1:c.2014C>T
|
ENSP00000513853.1:n.2014C>T
|
|
ENST00000698641.1:c.*1953C>T
|
ENSP00000513854.1:n.*1953C>T
|
|
ENST00000698642.1:c.*2182C>T
|
ENSP00000513855.1:n.*2182C>T
|
|
ENST00000698643.1:c.*2053C>T
|
ENSP00000513856.1:n.*2053C>T
|
|
ENST00000698644.1:c.2521C>T
|
ENSP00000513857.1:p.Arg841Trp
|
|
ENST00000698645.1:c.2731C>T
|
ENSP00000513858.1:p.Arg911Trp
|
|
ENST00000698646.1:c.2629C>T
|
ENSP00000513859.1:p.Arg877Trp
|
|
ENST00000698647.1:c.*2350C>T
|
ENSP00000513860.1:n.*2350C>T
|
|
ENST00000698648.1:c.*2136C>T
|
ENSP00000513862.1:n.*2136C>T
|
|
ENST00000698649.1:n.1733C>T
|
|
