ENST00000413910.6:c.1026A>C
|
ENSP00000400542.2:p.Leu342Phe
|
|
ENST00000426673.6:c.*529A>C
|
ENSP00000407253.3:n.*529A>C
|
|
ENST00000484317.6:n.931A>C
|
|
|
ENST00000696575.1:c.1146A>C
|
ENSP00000512730.1:p.Leu382Phe
|
|
ENST00000696577.1:c.1146A>C
|
ENSP00000512731.1:p.Leu382Phe
|
|
ENST00000696578.1:c.*98A>C
|
ENSP00000512732.1:n.*98A>C
|
|
ENST00000696579.1:n.1248A>C
|
|
|
ENST00000696580.1:c.1059A>C
|
ENSP00000512733.1:p.Leu353Phe
|
|
ENST00000696581.1:c.*1120A>C
|
ENSP00000512734.1:n.*1120A>C
|
|
ENST00000696582.1:c.*352A>C
|
ENSP00000512735.1:n.*352A>C
|
|
ENST00000696583.1:c.1107A>C
|
ENSP00000512736.1:p.Leu369Phe
|
|
ENST00000696584.1:n.1670A>C
|
|
|
ENST00000696585.1:n.1789A>C
|
|
|
ENST00000696586.1:n.1563A>C
|
|
|
ENST00000696587.1:c.1026A>C
|
ENSP00000512737.1:p.Leu342Phe
|
|
ENST00000696588.1:c.537A>C
|
ENSP00000513251.1:p.Leu179Phe
|
|
ENST00000696589.1:n.921A>C
|
|
|
ENST00000696590.1:n.770A>C
|
|
|
ENST00000696591.1:n.495A>C
|
|
|
ENST00000696592.1:n.2025A>C
|
|
|
ENST00000696627.1:c.1146A>C
|
ENSP00000512764.1:p.Leu382Phe
|
|
ENST00000696628.1:c.1146A>C
|
ENSP00000512765.1:p.Leu382Phe
|
|
ENST00000369550.10:c.1146A>C
MANE Select
|
ENSP00000358563.5:p.Leu382Phe
|
|
ENST00000369550.9:c.1146A>C
|
ENSP00000358563.5:p.Leu382Phe
|
|
ENST00000412124.5:c.404A>C
|
|
|
ENST00000426673.5:c.506A>C
|
|
|
ENST00000475966.1:n.635A>C
|
|
|
ENST00000481062.1:n.97A>C
|
|
|
ENST00000620277.4:c.1146A>C
|
ENSP00000478387.1:p.Leu382Phe
|
|
NM_001142463.2:c.1146A>C
|
NP_001135935.1:p.Leu382Phe
|
|
NM_001288747.1:c.1146A>C
|
NP_001275676.1:p.Leu382Phe
|
|
NM_001363.4:c.1146A>C
|
NP_001354.1:p.Leu382Phe
|
|
NR_110021.1:n.1847A>C
|
|
|
NR_110022.1:n.1966A>C
|
|
|
NR_110023.1:n.1740A>C
|
|
|
NM_001363.5:c.1146A>C
MANE Select
|
NP_001354.1:p.Leu382Phe
|
|
NM_001142463.3:c.1146A>C
|
NP_001135935.1:p.Leu382Phe
|
|
NR_110021.2:n.1725A>C
|
|
|
NR_110022.2:n.1844A>C
|
|
|
NR_110023.2:n.1618A>C
|
|
|
NM_001288747.2:c.1146A>C
|
NP_001275676.1:p.Leu382Phe
|
|