|
ENST00000371375.2:n.4434A>C
|
ENSP00000360426.1:p.Arg1478Ser
|
|
|
ENST00000685253.1:c.*1901A>C
|
ENSP00000509405.1:n.*1901A>C
|
|
|
ENST00000685889.1:n.2093A>C
|
|
|
|
ENST00000686807.1:n.777A>C
|
|
|
|
ENST00000686954.1:c.*642A>C
|
ENSP00000508416.1:n.*642A>C
|
|
|
ENST00000688810.1:n.4386A>C
|
ENSP00000509140.1:p.Arg1462Ser
|
|
|
ENST00000689233.1:n.9566A>C
|
|
|
|
ENST00000690340.1:n.3031A>C
|
|
|
|
ENST00000692286.1:c.5226A>C
|
ENSP00000509490.1:p.Arg1742Ser
|
|
|
ENST00000692396.1:c.5310A>C
|
ENSP00000508605.1:p.Arg1770Ser
|
|
|
ENST00000371380.8:c.5358A>C
MANE Select
|
ENSP00000360431.2:p.Arg1786Ser
|
|
|
ENST00000371385.8:c.4332A>C
|
ENSP00000360438.4:p.Arg1444Ser
|
|
|
ENST00000674738.1:n.3913A>C
|
|
|
|
ENST00000674827.1:n.3474A>C
|
ENSP00000502523.1:p.Arg1158Ser
|
|
|
ENST00000675218.1:n.4434A>C
|
ENSP00000501910.1:p.Arg1478Ser
|
|
|
ENST00000675487.1:c.*1291A>C
|
ENSP00000502340.1:n.*1291A>C
|
|
|
ENST00000675718.1:n.4627A>C
|
|
|
|
ENST00000260766.7:c.5358A>C
|
ENSP00000260766.3:p.Arg1786Ser
|
|
|
ENST00000371375.1:n.4434A>C
|
ENSP00000360426.1:p.Arg1478Ser
|
|
|
ENST00000371380.7:c.5358A>C
|
ENSP00000360431.2:p.Arg1786Ser
|
|
|
ENST00000371385.7:c.4434A>C
|
ENSP00000360438.3:p.Arg1478Ser
|
|
|
NM_001165979.2:c.4434A>C
|
NP_001159451.1:p.Arg1478Ser
|
|
|
NM_001288989.1:c.5310A>C
|
NP_001275918.1:p.Arg1770Ser
|
|
|
NM_016341.3:c.5358A>C
|
NP_057425.3:p.Arg1786Ser
|
|
|
XM_006717885.2:c.5400A>C
|
XP_006717948.1:p.Arg1800Ser
|
|
|
XM_006717886.2:c.5400A>C
|
XP_006717949.1:p.Arg1800Ser
|
|
|
XM_006717888.2:c.5397A>C
|
XP_006717951.1:p.Arg1799Ser
|
|
|
XM_006717889.2:c.5352A>C
|
XP_006717952.1:p.Arg1784Ser
|
|
|
XM_006717890.1:c.4476A>C
|
XP_006717953.1:p.Arg1492Ser
|
|
|
XM_011539849.1:c.5400A>C
|
XP_011538151.1:p.Arg1800Ser
|
|
|
XM_011539850.1:c.4245A>C
|
XP_011538152.1:p.Arg1415Ser
|
|
|
XM_006717885.4:c.5400A>C
|
XP_006717948.1:p.Arg1800Ser
|
|
|
XM_006717888.4:c.5397A>C
|
XP_006717951.1:p.Arg1799Ser
|
|
|
XM_006717889.4:c.5352A>C
|
XP_006717952.1:p.Arg1784Ser
|
|
|
XM_006717890.3:c.4476A>C
|
XP_006717953.1:p.Arg1492Ser
|
|
|
XM_011539849.3:c.5400A>C
|
XP_011538151.1:p.Arg1800Ser
|
|
|
XM_011539850.3:c.4245A>C
|
XP_011538152.1:p.Arg1415Ser
|
|
|
XM_017016310.2:c.5400A>C
|
XP_016871799.1:p.Arg1800Ser
|
|
|
XM_017016311.2:c.5400A>C
|
XP_016871800.1:p.Arg1800Ser
|
|
|
XM_017016312.2:c.4386A>C
|
XP_016871801.1:p.Arg1462Ser
|
|
|
NM_001288989.2:c.5310A>C
|
NP_001275918.1:p.Arg1770Ser
|
|
|
NM_016341.4:c.5358A>C
MANE Select
|
NP_057425.3:p.Arg1786Ser
|
|
