|
ENST00000703936.1:c.2771T>C
|
ENSP00000515567.1:p.Leu924Pro
|
|
|
ENST00000703937.1:c.*1832T>C
|
ENSP00000515568.1:n.*1832T>C
|
|
|
ENST00000326739.9:c.731T>C
MANE Select
|
ENSP00000321584.4:p.Leu244Pro
|
|
|
ENST00000429182.6:c.731T>C
|
ENSP00000393525.2:p.Leu244Pro
|
|
|
ENST00000442157.2:c.656T>C
|
ENSP00000403502.2:p.Leu219Pro
|
|
|
ENST00000462980.2:n.1246T>C
|
|
|
|
ENST00000472328.2:n.797T>C
|
|
|
|
ENST00000491610.2:n.691T>C
|
|
|
|
ENST00000676607.1:n.1027T>C
|
|
|
|
ENST00000676627.1:n.1461T>C
|
|
|
|
ENST00000676708.1:n.2011T>C
|
|
|
|
ENST00000676864.1:n.1880T>C
|
|
|
|
ENST00000677010.1:c.767T>C
|
ENSP00000503089.1:p.Leu256Pro
|
|
|
ENST00000677108.1:n.2637T>C
|
|
|
|
ENST00000677168.1:n.1203T>C
|
|
|
|
ENST00000677185.1:n.1294T>C
|
|
|
|
ENST00000677205.1:n.1515T>C
|
|
|
|
ENST00000677344.1:n.2005T>C
|
|
|
|
ENST00000677480.1:c.*408T>C
|
ENSP00000504378.1:n.*408T>C
|
|
|
ENST00000677519.1:n.1441T>C
|
|
|
|
ENST00000677593.1:n.1287T>C
|
|
|
|
ENST00000677740.1:n.2236T>C
|
|
|
|
ENST00000677991.1:n.1904T>C
|
|
|
|
ENST00000678001.1:n.1224T>C
|
|
|
|
ENST00000678085.1:n.1287T>C
|
|
|
|
ENST00000678177.1:n.2580T>C
|
|
|
|
ENST00000678603.1:n.1809T>C
|
|
|
|
ENST00000678724.1:c.656T>C
|
ENSP00000503874.1:p.Leu219Pro
|
|
|
ENST00000678920.1:n.889T>C
|
|
|
|
ENST00000679019.1:n.1501T>C
|
|
|
|
ENST00000679117.1:c.*546T>C
|
ENSP00000503240.1:n.*546T>C
|
|
|
ENST00000679339.1:n.1572T>C
|
|
|
|
ENST00000326739.8:c.731T>C
|
ENSP00000321584.4:p.Leu244Pro
|
|
|
ENST00000429182.5:c.525T>C
|
|
|
|
ENST00000442157.1:c.656T>C
|
ENSP00000403502.1:p.Leu219Pro
|
|
|
ENST00000462980.1:n.633T>C
|
|
|
|
ENST00000491610.1:n.691T>C
|
|
|
|
NM_000884.2:c.731T>C
|
NP_000875.2:p.Leu244Pro
|
|
|
XM_006713128.2:c.941T>C
|
XP_006713191.1:p.Leu314Pro
|
|
|
XM_006713128.3:c.941T>C
|
XP_006713191.1:p.Leu314Pro
|
|
|
XM_017006349.1:c.866T>C
|
XP_016861838.1:p.Leu289Pro
|
|
|
XM_017006350.1:c.866T>C
|
XP_016861839.1:p.Leu289Pro
|
|
|
NM_000884.3:c.731T>C
MANE Select
|
NP_000875.2:p.Leu244Pro
|
|
