ENST00000367099.4:n.1532T>C
|
|
|
ENST00000471071.2:c.272T>C
|
ENSP00000493073.2:p.Ile91Thr
|
|
ENST00000640756.2:n.337T>C
|
|
|
ENST00000659065.2:c.410T>C
|
ENSP00000499588.1:p.Ile137Thr
|
|
ENST00000659642.2:c.410T>C
|
ENSP00000499509.1:p.Ile137Thr
|
|
ENST00000664374.2:c.410T>C
|
ENSP00000499664.1:p.Ile137Thr
|
|
ENST00000640756.1:n.326T>C
|
|
|
ENST00000659065.1:c.410T>C
|
ENSP00000499588.1:p.Ile137Thr
|
|
ENST00000659642.1:c.410T>C
|
ENSP00000499509.1:p.Ile137Thr
|
|
ENST00000664374.1:c.410T>C
|
ENSP00000499664.1:p.Ile137Thr
|
|
ENST00000423557.1:c.527T>C
MANE Select
|
ENSP00000412237.1:p.Ile176Thr
|
|
NM_000572.2:c.527T>C
|
NP_000563.1:p.Ile176Thr
|
|
XM_011509506.1:c.527T>C
|
XP_011507808.1:p.Ile176Thr
|
|
NM_000572.3:c.527T>C
MANE Select
|
NP_000563.1:p.Ile176Thr
|
|
NM_001382624.1:c.272T>C
|
NP_001369553.1:p.Ile91Thr
|
|
NR_168466.1:n.824T>C
|
|
|
NR_168467.1:n.354T>C
|
|
|