ENST00000413910.6:c.989T>C
|
ENSP00000400542.2:p.Ile330Thr
|
|
ENST00000426673.6:c.*492T>C
|
ENSP00000407253.3:n.*492T>C
|
|
ENST00000484317.6:n.894T>C
|
|
|
ENST00000696575.1:c.1109T>C
|
ENSP00000512730.1:p.Ile370Thr
|
|
ENST00000696577.1:c.1109T>C
|
ENSP00000512731.1:p.Ile370Thr
|
|
ENST00000696578.1:c.*61T>C
|
ENSP00000512732.1:n.*61T>C
|
|
ENST00000696579.1:n.1211T>C
|
|
|
ENST00000696580.1:c.1022T>C
|
ENSP00000512733.1:p.Ile341Thr
|
|
ENST00000696581.1:c.*1083T>C
|
ENSP00000512734.1:n.*1083T>C
|
|
ENST00000696582.1:c.*315T>C
|
ENSP00000512735.1:n.*315T>C
|
|
ENST00000696583.1:c.1070T>C
|
ENSP00000512736.1:p.Ile357Thr
|
|
ENST00000696584.1:n.1633T>C
|
|
|
ENST00000696585.1:n.1752T>C
|
|
|
ENST00000696586.1:n.1526T>C
|
|
|
ENST00000696587.1:c.989T>C
|
ENSP00000512737.1:p.Ile330Thr
|
|
ENST00000696588.1:c.500T>C
|
ENSP00000513251.1:p.Ile167Thr
|
|
ENST00000696589.1:n.884T>C
|
|
|
ENST00000696590.1:n.733T>C
|
|
|
ENST00000696591.1:n.458T>C
|
|
|
ENST00000696592.1:n.1988T>C
|
|
|
ENST00000696627.1:c.1109T>C
|
ENSP00000512764.1:p.Ile370Thr
|
|
ENST00000696628.1:c.1109T>C
|
ENSP00000512765.1:p.Ile370Thr
|
|
ENST00000369550.10:c.1109T>C
MANE Select
|
ENSP00000358563.5:p.Ile370Thr
|
|
ENST00000369550.9:c.1109T>C
|
ENSP00000358563.5:p.Ile370Thr
|
|
ENST00000412124.5:c.367T>C
|
|
|
ENST00000426673.5:c.469T>C
|
|
|
ENST00000475966.1:n.598T>C
|
|
|
ENST00000481062.1:n.60T>C
|
|
|
ENST00000620277.4:c.1109T>C
|
ENSP00000478387.1:p.Ile370Thr
|
|
NM_001142463.2:c.1109T>C
|
NP_001135935.1:p.Ile370Thr
|
|
NM_001288747.1:c.1109T>C
|
NP_001275676.1:p.Ile370Thr
|
|
NM_001363.4:c.1109T>C
|
NP_001354.1:p.Ile370Thr
|
|
NR_110021.1:n.1810T>C
|
|
|
NR_110022.1:n.1929T>C
|
|
|
NR_110023.1:n.1703T>C
|
|
|
NM_001363.5:c.1109T>C
MANE Select
|
NP_001354.1:p.Ile370Thr
|
|
NM_001142463.3:c.1109T>C
|
NP_001135935.1:p.Ile370Thr
|
|
NR_110021.2:n.1688T>C
|
|
|
NR_110022.2:n.1807T>C
|
|
|
NR_110023.2:n.1581T>C
|
|
|
NM_001288747.2:c.1109T>C
|
NP_001275676.1:p.Ile370Thr
|
|