ENST00000703936.1:c.2859G>T
|
ENSP00000515567.1:p.Leu953Phe
|
|
ENST00000703937.1:c.*1920G>T
|
ENSP00000515568.1:n.*1920G>T
|
|
ENST00000326739.9:c.819G>T
MANE Select
|
ENSP00000321584.4:p.Leu273Phe
|
|
ENST00000429182.6:c.819G>T
|
ENSP00000393525.2:p.Leu273Phe
|
|
ENST00000442157.2:c.744G>T
|
ENSP00000403502.2:p.Leu248Phe
|
|
ENST00000462980.2:n.1334G>T
|
|
|
ENST00000472328.2:n.885G>T
|
|
|
ENST00000491610.2:n.779G>T
|
|
|
ENST00000676607.1:n.1115G>T
|
|
|
ENST00000676627.1:n.1549G>T
|
|
|
ENST00000676708.1:n.2099G>T
|
|
|
ENST00000676864.1:n.1968G>T
|
|
|
ENST00000677010.1:c.855G>T
|
ENSP00000503089.1:p.Leu285Phe
|
|
ENST00000677108.1:n.2725G>T
|
|
|
ENST00000677168.1:n.1291G>T
|
|
|
ENST00000677185.1:n.1382G>T
|
|
|
ENST00000677205.1:n.1603G>T
|
|
|
ENST00000677344.1:n.2093G>T
|
|
|
ENST00000677480.1:c.*496G>T
|
ENSP00000504378.1:n.*496G>T
|
|
ENST00000677519.1:n.1529G>T
|
|
|
ENST00000677593.1:n.1375G>T
|
|
|
ENST00000677740.1:n.2324G>T
|
|
|
ENST00000677991.1:n.1992G>T
|
|
|
ENST00000678001.1:n.1312G>T
|
|
|
ENST00000678085.1:n.1375G>T
|
|
|
ENST00000678177.1:n.2668G>T
|
|
|
ENST00000678603.1:n.1897G>T
|
|
|
ENST00000678724.1:c.744G>T
|
ENSP00000503874.1:p.Leu248Phe
|
|
ENST00000678920.1:n.977G>T
|
|
|
ENST00000679019.1:n.1589G>T
|
|
|
ENST00000679117.1:c.*634G>T
|
ENSP00000503240.1:n.*634G>T
|
|
ENST00000679339.1:n.1660G>T
|
|
|
ENST00000326739.8:c.819G>T
|
ENSP00000321584.4:p.Leu273Phe
|
|
ENST00000429182.5:c.613G>T
|
|
|
ENST00000442157.1:c.744G>T
|
ENSP00000403502.1:p.Leu248Phe
|
|
ENST00000462980.1:n.721G>T
|
|
|
ENST00000491610.1:n.779G>T
|
|
|
NM_000884.2:c.819G>T
|
NP_000875.2:p.Leu273Phe
|
|
XM_006713128.2:c.1029G>T
|
XP_006713191.1:p.Leu343Phe
|
|
XM_006713128.3:c.1029G>T
|
XP_006713191.1:p.Leu343Phe
|
|
XM_017006349.1:c.954G>T
|
XP_016861838.1:p.Leu318Phe
|
|
XM_017006350.1:c.954G>T
|
XP_016861839.1:p.Leu318Phe
|
|
NM_000884.3:c.819G>T
MANE Select
|
NP_000875.2:p.Leu273Phe
|
|