ENST00000425815.6:c.2816G>C
|
ENSP00000394410.2:p.Arg939Thr
|
|
ENST00000430374.6:c.2816G>C
|
ENSP00000405077.2:p.Arg939Thr
|
|
ENST00000444508.6:c.2816G>C
|
ENSP00000398969.2:p.Arg939Thr
|
|
ENST00000697899.1:c.2582G>C
|
ENSP00000513470.1:p.Arg861Thr
|
|
ENST00000697901.1:c.*1571G>C
|
ENSP00000513471.1:n.*1571G>C
|
|
ENST00000697903.1:c.*1303G>C
|
ENSP00000513472.1:n.*1303G>C
|
|
ENST00000697904.1:c.*1303G>C
|
ENSP00000513473.1:n.*1303G>C
|
|
ENST00000697905.1:c.*1303G>C
|
ENSP00000513474.1:n.*1303G>C
|
|
ENST00000697906.1:c.2582G>C
|
ENSP00000513475.1:p.Arg861Thr
|
|
ENST00000697907.1:c.*1674G>C
|
ENSP00000513476.1:n.*1674G>C
|
|
ENST00000697909.1:n.1708G>C
|
|
|
ENST00000697910.1:n.1213G>C
|
|
|
ENST00000357276.9:c.2816G>C
MANE Select
|
ENSP00000349823.4:p.Arg939Thr
|
|
ENST00000357276.8:c.2816G>C
|
ENSP00000349823.4:p.Arg939Thr
|
|
ENST00000358207.9:c.2816G>C
|
ENSP00000350940.5:p.Arg939Thr
|
|
ENST00000392128.6:c.2342G>C
|
ENSP00000375974.2:p.Arg781Thr
|
|
NM_001127207.1:c.2816G>C
|
NP_001120679.1:p.Arg939Thr
|
|
NM_014140.3:c.2816G>C , LRG_108t1:c.2816G>C
|
NP_054859.2:p.Arg939Thr
|
|
XM_005246631.2:c.2816G>C
|
XP_005246688.1:p.Arg939Thr
|
|
XM_005246632.1:c.2816G>C
|
XP_005246689.1:p.Arg939Thr
|
|
XM_006712557.1:c.2750G>C
|
XP_006712620.1:p.Arg917Thr
|
|
XM_005246632.2:c.2816G>C
|
XP_005246689.1:p.Arg939Thr
|
|
XM_017004228.2:c.1904G>C
|
XP_016859717.1:p.Arg635Thr
|
|
NM_001127207.2:c.2816G>C
|
NP_001120679.1:p.Arg939Thr
|
|
NM_014140.4:c.2816G>C
MANE Select
|
NP_054859.2:p.Arg939Thr
|
|