|
ENST00000703936.1:c.2648G>C
|
ENSP00000515567.1:p.Arg883Pro
|
|
|
ENST00000703937.1:c.*1709G>C
|
ENSP00000515568.1:n.*1709G>C
|
|
|
ENST00000326739.9:c.608G>C
MANE Select
|
ENSP00000321584.4:p.Arg203Pro
|
|
|
ENST00000429182.6:c.608G>C
|
ENSP00000393525.2:p.Arg203Pro
|
|
|
ENST00000442157.2:c.533G>C
|
ENSP00000403502.2:p.Arg178Pro
|
|
|
ENST00000462980.2:n.1123G>C
|
|
|
|
ENST00000472328.2:n.674G>C
|
|
|
|
ENST00000491610.2:n.495G>C
|
|
|
|
ENST00000676607.1:n.904G>C
|
|
|
|
ENST00000676627.1:n.1338G>C
|
|
|
|
ENST00000676708.1:n.1815G>C
|
|
|
|
ENST00000676864.1:n.1684G>C
|
|
|
|
ENST00000677010.1:c.644G>C
|
ENSP00000503089.1:p.Arg215Pro
|
|
|
ENST00000677108.1:n.2441G>C
|
|
|
|
ENST00000677168.1:n.1080G>C
|
|
|
|
ENST00000677185.1:n.1098G>C
|
|
|
|
ENST00000677205.1:n.1319G>C
|
|
|
|
ENST00000677344.1:n.1809G>C
|
|
|
|
ENST00000677480.1:c.*285G>C
|
ENSP00000504378.1:n.*285G>C
|
|
|
ENST00000677519.1:n.1318G>C
|
|
|
|
ENST00000677593.1:n.1091G>C
|
|
|
|
ENST00000677740.1:n.2040G>C
|
|
|
|
ENST00000677991.1:n.1781G>C
|
|
|
|
ENST00000678001.1:n.1101G>C
|
|
|
|
ENST00000678085.1:n.1091G>C
|
|
|
|
ENST00000678177.1:n.2384G>C
|
|
|
|
ENST00000678603.1:n.1686G>C
|
|
|
|
ENST00000678724.1:c.533G>C
|
ENSP00000503874.1:p.Arg178Pro
|
|
|
ENST00000678920.1:n.766G>C
|
|
|
|
ENST00000679019.1:n.1305G>C
|
|
|
|
ENST00000679117.1:c.*423G>C
|
ENSP00000503240.1:n.*423G>C
|
|
|
ENST00000679339.1:n.1376G>C
|
|
|
|
ENST00000326739.8:c.608G>C
|
ENSP00000321584.4:p.Arg203Pro
|
|
|
ENST00000429182.5:c.402G>C
|
|
|
|
ENST00000442157.1:c.533G>C
|
ENSP00000403502.1:p.Arg178Pro
|
|
|
ENST00000462980.1:n.510G>C
|
|
|
|
ENST00000491610.1:n.495G>C
|
|
|
|
NM_000884.2:c.608G>C
|
NP_000875.2:p.Arg203Pro
|
|
|
XM_006713128.2:c.818G>C
|
XP_006713191.1:p.Arg273Pro
|
|
|
XM_006713128.3:c.818G>C
|
XP_006713191.1:p.Arg273Pro
|
|
|
XM_017006349.1:c.743G>C
|
XP_016861838.1:p.Arg248Pro
|
|
|
XM_017006350.1:c.743G>C
|
XP_016861839.1:p.Arg248Pro
|
|
|
NM_000884.3:c.608G>C
MANE Select
|
NP_000875.2:p.Arg203Pro
|
|
