ENST00000703936.1:c.2712G>T
|
ENSP00000515567.1:p.Arg904=
|
|
ENST00000703937.1:c.*1773G>T
|
ENSP00000515568.1:n.*1773G>T
|
|
ENST00000326739.9:c.672G>T
MANE Select
|
ENSP00000321584.4:p.Arg224=
|
|
ENST00000429182.6:c.672G>T
|
ENSP00000393525.2:p.Arg224=
|
|
ENST00000442157.2:c.597G>T
|
ENSP00000403502.2:p.Arg199=
|
|
ENST00000462980.2:n.1187G>T
|
|
|
ENST00000472328.2:n.738G>T
|
|
|
ENST00000491610.2:n.632G>T
|
|
|
ENST00000676607.1:n.968G>T
|
|
|
ENST00000676627.1:n.1402G>T
|
|
|
ENST00000676708.1:n.1952G>T
|
|
|
ENST00000676864.1:n.1821G>T
|
|
|
ENST00000677010.1:c.708G>T
|
ENSP00000503089.1:p.Arg236=
|
|
ENST00000677108.1:n.2578G>T
|
|
|
ENST00000677168.1:n.1144G>T
|
|
|
ENST00000677185.1:n.1235G>T
|
|
|
ENST00000677205.1:n.1456G>T
|
|
|
ENST00000677344.1:n.1946G>T
|
|
|
ENST00000677480.1:c.*349G>T
|
ENSP00000504378.1:n.*349G>T
|
|
ENST00000677519.1:n.1382G>T
|
|
|
ENST00000677593.1:n.1228G>T
|
|
|
ENST00000677740.1:n.2177G>T
|
|
|
ENST00000677991.1:n.1845G>T
|
|
|
ENST00000678001.1:n.1165G>T
|
|
|
ENST00000678085.1:n.1228G>T
|
|
|
ENST00000678177.1:n.2521G>T
|
|
|
ENST00000678603.1:n.1750G>T
|
|
|
ENST00000678724.1:c.597G>T
|
ENSP00000503874.1:p.Arg199=
|
|
ENST00000678920.1:n.830G>T
|
|
|
ENST00000679019.1:n.1442G>T
|
|
|
ENST00000679117.1:c.*487G>T
|
ENSP00000503240.1:n.*487G>T
|
|
ENST00000679339.1:n.1513G>T
|
|
|
ENST00000326739.8:c.672G>T
|
ENSP00000321584.4:p.Arg224=
|
|
ENST00000429182.5:c.466G>T
|
|
|
ENST00000442157.1:c.597G>T
|
ENSP00000403502.1:p.Arg199=
|
|
ENST00000462980.1:n.574G>T
|
|
|
ENST00000491610.1:n.632G>T
|
|
|
NM_000884.2:c.672G>T
|
NP_000875.2:p.Arg224=
|
|
XM_006713128.2:c.882G>T
|
XP_006713191.1:p.Arg294=
|
|
XM_006713128.3:c.882G>T
|
XP_006713191.1:p.Arg294=
|
|
XM_017006349.1:c.807G>T
|
XP_016861838.1:p.Arg269=
|
|
XM_017006350.1:c.807G>T
|
XP_016861839.1:p.Arg269=
|
|
NM_000884.3:c.672G>T
MANE Select
|
NP_000875.2:p.Arg224=
|
|