|
NM_001394998.1:c.5650C>T
MANE Select
|
NP_001381927.1:p.Arg1884Trp
|
|
ENST00000689528.1:c.5650C>T
MANE Select
|
ENSP00000510600.1:p.Arg1884Trp
|
|
NM_025185.3:c.5398C>T
|
NP_079461.2:p.Arg1800Trp
|
|
NM_025185.4:c.5398C>T
|
NP_079461.2:p.Arg1800Trp
|
|
ENST00000389520.8:c.5428C>T
|
ENSP00000374171.4:p.Arg1810Trp
|
|
ENST00000424789.6:c.5398C>T
|
ENSP00000387593.2:p.Arg1800Trp
|
|
ENST00000583356.5:c.5083C>T
|
|
|
ENST00000613171.4:c.2728C>T
|
ENSP00000478576.1:p.Arg910Trp
|
|
XM_005257203.3:c.5398C>T
|
XP_005257260.1:p.Arg1800Trp
|
|
XM_005257203.4:c.5398C>T
|
XP_005257260.1:p.Arg1800Trp
|
|
XM_006721806.2:c.5650C>T
|
XP_006721869.1:p.Arg1884Trp
|
|
XM_006721806.3:c.5650C>T
|
XP_006721869.1:p.Arg1884Trp
|
|
XM_006721807.2:c.5620C>T
|
XP_006721870.1:p.Arg1874Trp
|
|
XM_006721807.3:c.5620C>T
|
XP_006721870.1:p.Arg1874Trp
|
|
XM_006721811.2:c.*1319C>T
|
XP_006721874.1:n.*1319C>T
|
|
XM_006721811.4:c.*1319C>T
|
XP_006721874.1:n.*1319C>T
|
|
XM_011524597.1:c.5653C>T
|
XP_011522899.1:p.Arg1885Trp
|
|
XM_011524597.2:c.5653C>T
|
XP_011522899.1:p.Arg1885Trp
|
|
XM_011524598.1:c.5623C>T
|
XP_011522900.1:p.Arg1875Trp
|
|
XM_011524598.2:c.5623C>T
|
XP_011522900.1:p.Arg1875Trp
|
|
XM_011524599.1:c.5605C>T
|
XP_011522901.1:p.Arg1869Trp
|
|
XM_011524600.1:c.5542C>T
|
XP_011522902.1:p.Arg1848Trp
|
|
XM_011524600.2:c.5542C>T
|
XP_011522902.1:p.Arg1848Trp
|
|
XM_011524601.1:c.5542C>T
|
XP_011522903.1:p.Arg1848Trp
|
|
XM_011524601.2:c.5542C>T
|
XP_011522903.1:p.Arg1848Trp
|
|
XM_011524602.1:c.5431C>T
|
XP_011522904.1:p.Arg1811Trp
|
|
XM_011524602.2:c.5431C>T
|
XP_011522904.1:p.Arg1811Trp
|
|
XM_011524603.1:c.5161C>T
|
XP_011522905.1:p.Arg1721Trp
|
|
XM_011524604.1:c.2503C>T
|
XP_011522906.1:p.Arg835Trp
|
|
XM_017024429.1:c.5572C>T
|
XP_016879918.1:p.Arg1858Trp
|
|
XM_017024430.2:c.5161C>T
|
XP_016879919.1:p.Arg1721Trp
|
