|
ENST00000703936.1:c.2671A>T
|
ENSP00000515567.1:p.Ile891Phe
|
|
|
ENST00000703937.1:c.*1732A>T
|
ENSP00000515568.1:n.*1732A>T
|
|
|
ENST00000326739.9:c.631A>T
MANE Select
|
ENSP00000321584.4:p.Ile211Phe
|
|
|
ENST00000429182.6:c.631A>T
|
ENSP00000393525.2:p.Ile211Phe
|
|
|
ENST00000442157.2:c.556A>T
|
ENSP00000403502.2:p.Ile186Phe
|
|
|
ENST00000462980.2:n.1146A>T
|
|
|
|
ENST00000472328.2:n.697A>T
|
|
|
|
ENST00000491610.2:n.591A>T
|
|
|
|
ENST00000676607.1:n.927A>T
|
|
|
|
ENST00000676627.1:n.1361A>T
|
|
|
|
ENST00000676708.1:n.1911A>T
|
|
|
|
ENST00000676864.1:n.1780A>T
|
|
|
|
ENST00000677010.1:c.667A>T
|
ENSP00000503089.1:p.Ile223Phe
|
|
|
ENST00000677108.1:n.2537A>T
|
|
|
|
ENST00000677168.1:n.1103A>T
|
|
|
|
ENST00000677185.1:n.1194A>T
|
|
|
|
ENST00000677205.1:n.1415A>T
|
|
|
|
ENST00000677344.1:n.1905A>T
|
|
|
|
ENST00000677480.1:c.*308A>T
|
ENSP00000504378.1:n.*308A>T
|
|
|
ENST00000677519.1:n.1341A>T
|
|
|
|
ENST00000677593.1:n.1187A>T
|
|
|
|
ENST00000677740.1:n.2136A>T
|
|
|
|
ENST00000677991.1:n.1804A>T
|
|
|
|
ENST00000678001.1:n.1124A>T
|
|
|
|
ENST00000678085.1:n.1187A>T
|
|
|
|
ENST00000678177.1:n.2480A>T
|
|
|
|
ENST00000678603.1:n.1709A>T
|
|
|
|
ENST00000678724.1:c.556A>T
|
ENSP00000503874.1:p.Ile186Phe
|
|
|
ENST00000678920.1:n.789A>T
|
|
|
|
ENST00000679019.1:n.1401A>T
|
|
|
|
ENST00000679117.1:c.*446A>T
|
ENSP00000503240.1:n.*446A>T
|
|
|
ENST00000679339.1:n.1472A>T
|
|
|
|
ENST00000326739.8:c.631A>T
|
ENSP00000321584.4:p.Ile211Phe
|
|
|
ENST00000429182.5:c.425A>T
|
|
|
|
ENST00000442157.1:c.556A>T
|
ENSP00000403502.1:p.Ile186Phe
|
|
|
ENST00000462980.1:n.533A>T
|
|
|
|
ENST00000491610.1:n.591A>T
|
|
|
|
NM_000884.2:c.631A>T
|
NP_000875.2:p.Ile211Phe
|
|
|
XM_006713128.2:c.841A>T
|
XP_006713191.1:p.Ile281Phe
|
|
|
XM_006713128.3:c.841A>T
|
XP_006713191.1:p.Ile281Phe
|
|
|
XM_017006349.1:c.766A>T
|
XP_016861838.1:p.Ile256Phe
|
|
|
XM_017006350.1:c.766A>T
|
XP_016861839.1:p.Ile256Phe
|
|
|
NM_000884.3:c.631A>T
MANE Select
|
NP_000875.2:p.Ile211Phe
|
|
