ENST00000351691.10:c.386T>C
|
ENSP00000332468.5:p.Met129Thr
|
|
ENST00000699893.1:c.386T>C
|
ENSP00000514677.1:p.Met129Thr
|
|
ENST00000699894.1:c.386T>C
|
ENSP00000514678.1:p.Met129Thr
|
|
ENST00000699895.1:n.516T>C
|
|
|
ENST00000699896.1:n.317T>C
|
|
|
ENST00000392745.8:c.386T>C
MANE Select
|
ENSP00000376500.3:p.Met129Thr
|
|
ENST00000347662.8:c.386T>C
|
ENSP00000328003.4:p.Met129Thr
|
|
ENST00000351691.9:c.386T>C
|
ENSP00000332468.5:p.Met129Thr
|
|
ENST00000392745.6:c.386T>C
|
ENSP00000376500.2:p.Met129Thr
|
|
ENST00000539721.5:c.386T>C
|
ENSP00000445998.1:p.Met129Thr
|
|
ENST00000558700.5:c.131T>C
|
ENSP00000453031.1:p.Met44Thr
|
|
ENST00000558880.1:n.38T>C
|
|
|
ENST00000559734.1:c.26T>C
|
ENSP00000453032.1:p.Met9Thr
|
|
ENST00000560371.5:c.386T>C
|
ENSP00000454207.1:p.Met129Thr
|
|
NM_001199427.1:c.386T>C
|
NP_001186356.1:p.Met129Thr
|
|
NM_003300.3:c.386T>C
|
NP_003291.2:p.Met129Thr
|
|
NM_145725.2:c.386T>C , LRG_229t1:c.386T>C
|
NP_663777.1:p.Met129Thr
|
|
NM_145726.2:c.386T>C
|
NP_663778.1:p.Met129Thr
|
|
XM_011537116.1:c.386T>C
|
XP_011535418.1:p.Met129Thr
|
|
XM_011537117.1:c.386T>C
|
XP_011535419.1:p.Met129Thr
|
|
XM_011537118.1:c.386T>C
|
XP_011535420.1:p.Met129Thr
|
|
XR_943512.1:n.743T>C
|
|
|
XM_011537116.3:c.386T>C
|
XP_011535418.1:p.Met129Thr
|
|
XM_011537117.3:c.386T>C
|
XP_011535419.1:p.Met129Thr
|
|
XM_011537118.3:c.386T>C
|
XP_011535420.1:p.Met129Thr
|
|
XM_017021617.1:c.386T>C
|
XP_016877106.1:p.Met129Thr
|
|
XM_017021618.1:c.386T>C
|
XP_016877107.1:p.Met129Thr
|
|
XM_017021619.1:c.386T>C
|
XP_016877108.1:p.Met129Thr
|
|
XM_017021620.2:c.386T>C
|
XP_016877109.1:p.Met129Thr
|
|
NM_001199427.2:c.386T>C
|
NP_001186356.1:p.Met129Thr
|
|
NM_003300.4:c.386T>C
|
NP_003291.2:p.Met129Thr
|
|
NM_145725.3:c.386T>C
MANE Select
|
NP_663777.1:p.Met129Thr
|
|
NM_001385142.1:c.386T>C
|
NP_001372071.1:p.Met129Thr
|
|
NM_001385143.1:c.386T>C
|
NP_001372072.1:p.Met129Thr
|
|
NM_145726.3:c.386T>C
|
NP_663778.1:p.Met129Thr
|
|