ENST00000369702.5:c.2088G>T
MANE Select
|
ENSP00000358716.4:p.Leu696Phe
|
|
ENST00000533164.6:c.*1502G>T
|
ENSP00000434085.1:n.*1502G>T
|
|
ENST00000534200.2:n.3823G>T
|
|
|
ENST00000679381.1:n.2710G>T
|
|
|
ENST00000679498.1:n.3946G>T
|
|
|
ENST00000679576.1:c.2423G>T
|
ENSP00000506357.1:n.2423G>T
|
|
ENST00000679724.1:c.2088G>T
|
ENSP00000505857.1:p.Leu696Phe
|
|
ENST00000679774.1:n.3713G>T
|
|
|
ENST00000680038.1:n.3080G>T
|
|
|
ENST00000680317.1:n.2436G>T
|
|
|
ENST00000680383.1:c.*967G>T
|
ENSP00000505119.1:n.*967G>T
|
|
ENST00000680415.1:n.3419G>T
|
|
|
ENST00000680518.1:c.*814G>T
|
ENSP00000506543.1:n.*814G>T
|
|
ENST00000680627.1:c.2088G>T
|
ENSP00000505758.1:p.Leu696Phe
|
|
ENST00000680936.1:c.*1316G>T
|
ENSP00000506651.1:n.*1316G>T
|
|
ENST00000680983.1:n.1957G>T
|
|
|
ENST00000681529.1:n.2810G>T
|
|
|
ENST00000681559.1:c.*1265G>T
|
ENSP00000506100.1:n.*1265G>T
|
|
ENST00000681747.1:n.3088G>T
|
|
|
ENST00000369702.4:c.2088G>T
|
ENSP00000358716.4:p.Leu696Phe
|
|
ENST00000475700.1:c.912G>T
|
ENSP00000435660.1:p.Leu304Phe
|
|
NM_007204.4:c.2088G>T
|
NP_009135.4:p.Leu696Phe
|
|
NM_007204.5:c.2088G>T
MANE Select
|
NP_009135.4:p.Leu696Phe
|
|