|
NM_001130987.2:c.5727G>T
MANE Select
|
NP_001124459.1:p.Arg1909Ser
|
|
ENST00000410020.8:c.5727G>T
MANE Select
|
ENSP00000386881.3:p.Arg1909Ser
|
|
NM_003494.4:c.5610G>T
MANE Plus Clinical
|
NP_003485.1:p.Arg1870Ser
|
|
ENST00000258104.8:c.5610G>T
MANE Plus Clinical
|
ENSP00000258104.3:p.Arg1870Ser
|
|
NM_001130455.1:c.5613G>T
|
NP_001123927.1:p.Arg1871Ser
|
|
NM_001130455.2:c.5613G>T
|
NP_001123927.1:p.Arg1871Ser
|
|
NM_001130976.1:c.5568G>T
|
NP_001124448.1:p.Arg1856Ser
|
|
NM_001130976.2:c.5568G>T
|
NP_001124448.1:p.Arg1856Ser
|
|
NM_001130977.1:c.5631G>T
|
NP_001124449.1:p.Arg1877Ser
|
|
NM_001130977.2:c.5631G>T
|
NP_001124449.1:p.Arg1877Ser
|
|
NM_001130978.1:c.5673G>T
|
NP_001124450.1:p.Arg1891Ser
|
|
NM_001130978.2:c.5673G>T
|
NP_001124450.1:p.Arg1891Ser
|
|
NM_001130979.1:c.5703G>T
|
NP_001124451.1:p.Arg1901Ser
|
|
NM_001130979.2:c.5703G>T
|
NP_001124451.1:p.Arg1901Ser
|
|
NM_001130980.1:c.5661G>T
|
NP_001124452.1:p.Arg1887Ser
|
|
NM_001130980.2:c.5661G>T
|
NP_001124452.1:p.Arg1887Ser
|
|
NM_001130981.1:c.5724G>T
|
NP_001124453.1:p.Arg1908Ser
|
|
NM_001130981.2:c.5724G>T
|
NP_001124453.1:p.Arg1908Ser
|
|
NM_001130982.1:c.5706G>T
|
NP_001124454.1:p.Arg1902Ser
|
|
NM_001130982.2:c.5706G>T
|
NP_001124454.1:p.Arg1902Ser
|
|
NM_001130983.1:c.5676G>T
|
NP_001124455.1:p.Arg1892Ser
|
|
NM_001130983.2:c.5676G>T
|
NP_001124455.1:p.Arg1892Ser
|
|
NM_001130984.1:c.5634G>T
|
NP_001124456.1:p.Arg1878Ser
|
|
NM_001130984.2:c.5634G>T
|
NP_001124456.1:p.Arg1878Ser
|
|
NM_001130985.1:c.5664G>T
|
NP_001124457.1:p.Arg1888Ser
|
|
NM_001130985.2:c.5664G>T
|
NP_001124457.1:p.Arg1888Ser
|
|
NM_001130986.1:c.5571G>T
|
NP_001124458.1:p.Arg1857Ser
|
|
NM_001130986.2:c.5571G>T
|
NP_001124458.1:p.Arg1857Ser
|
|
NM_001130987.1:c.5727G>T
|
NP_001124459.1:p.Arg1909Ser
|
|
NM_003494.3:c.5610G>T
|
NP_003485.1:p.Arg1870Ser
|
|
ENST00000258104.7:c.5610G>T
|
ENSP00000258104.3:p.Arg1870Ser
|
|
ENST00000394120.6:c.5613G>T
|
ENSP00000377678.2:p.Arg1871Ser
|
|
ENST00000409366.5:c.5676G>T
|
ENSP00000386512.1:p.Arg1892Ser
|
|
ENST00000409582.7:c.5724G>T
|
ENSP00000386547.3:p.Arg1908Ser
|
|
ENST00000409651.5:c.5706G>T
|
ENSP00000386683.1:p.Arg1902Ser
|
|
ENST00000409744.5:c.5634G>T
|
ENSP00000386285.1:p.Arg1878Ser
|
|
ENST00000409762.5:c.5661G>T
|
ENSP00000387137.1:p.Arg1887Ser
|
|
ENST00000410020.7:c.5727G>T
|
ENSP00000386881.3:p.Arg1909Ser
|
|
ENST00000410041.1:c.5664G>T
|
ENSP00000386617.1:p.Arg1888Ser
|
|
ENST00000413539.6:c.5703G>T
|
ENSP00000407046.2:p.Arg1901Ser
|
|
ENST00000429174.6:c.5673G>T
|
ENSP00000398305.2:p.Arg1891Ser
|
|
ENST00000479049.6:n.2495G>T
|
|
|
ENST00000698057.1:c.3141G>T
|
ENSP00000513536.1:p.Arg1047Ser
|
|
ENST00000698058.1:c.2358G>T
|
ENSP00000513537.1:p.Arg786Ser
|
|
ENST00000698059.1:c.2466G>T
|
ENSP00000513538.1:p.Arg822Ser
|
|
XM_005264584.3:c.5769G>T
|
XP_005264641.1:p.Arg1923Ser
|
|
XM_005264584.4:c.5769G>T
|
XP_005264641.1:p.Arg1923Ser
|
|
XM_005264585.3:c.5766G>T
|
XP_005264642.1:p.Arg1922Ser
|
|
XM_005264585.5:c.5766G>T
|
XP_005264642.1:p.Arg1922Ser
|
