ENST00000357060.8:c.3410G>C
MANE Select
|
ENSP00000349568.3:p.Arg1137Thr
|
|
ENST00000357060.7:c.3410G>C
|
ENSP00000349568.3:p.Arg1137Thr
|
|
ENST00000434629.5:c.1492G>C
|
|
|
NM_025145.5:c.3410G>C
|
NP_079421.5:p.Arg1137Thr
|
|
XM_005270171.1:c.3413G>C
|
XP_005270228.1:p.Arg1138Thr
|
|
XM_005270172.2:c.3413G>C
|
XP_005270229.1:p.Arg1138Thr
|
|
XM_011540196.1:c.3527G>C
|
XP_011538498.1:p.Arg1176Thr
|
|
XM_011540197.1:c.3527G>C
|
XP_011538499.1:p.Arg1176Thr
|
|
XM_011540198.1:c.3410G>C
|
XP_011538500.1:p.Arg1137Thr
|
|
XM_011540199.1:c.3410G>C
|
XP_011538501.1:p.Arg1137Thr
|
|
XM_011540200.1:c.3527G>C
|
XP_011538502.1:p.Arg1176Thr
|
|
XM_011540201.1:c.3527G>C
|
XP_011538503.1:p.Arg1176Thr
|
|
XM_011540202.1:c.2756G>C
|
XP_011538504.1:p.Arg919Thr
|
|
XM_011540203.1:c.1310G>C
|
XP_011538505.1:p.Arg437Thr
|
|
NM_025145.6:c.3410G>C
|
NP_079421.5:p.Arg1137Thr
|
|
XM_005270171.2:c.3413G>C
|
XP_005270228.1:p.Arg1138Thr
|
|
XM_005270172.3:c.3413G>C
|
XP_005270229.1:p.Arg1138Thr
|
|
XM_011540196.2:c.3527G>C
|
XP_011538498.1:p.Arg1176Thr
|
|
XM_011540197.2:c.3527G>C
|
XP_011538499.1:p.Arg1176Thr
|
|
XM_011540198.2:c.3410G>C
|
XP_011538500.1:p.Arg1137Thr
|
|
XM_011540199.2:c.3410G>C
|
XP_011538501.1:p.Arg1137Thr
|
|
XM_011540200.2:c.3527G>C
|
XP_011538502.1:p.Arg1176Thr
|
|
XM_011540201.2:c.3527G>C
|
XP_011538503.1:p.Arg1176Thr
|
|
XM_011540202.2:c.2756G>C
|
XP_011538504.1:p.Arg919Thr
|
|
XM_017016681.1:c.3524G>C
|
XP_016872170.1:p.Arg1175Thr
|
|
XM_017016682.1:c.3179G>C
|
XP_016872171.1:p.Arg1060Thr
|
|
XM_024448177.1:c.1913G>C
|
XP_024303945.1:p.Arg638Thr
|
|
XM_024448178.1:c.1310G>C
|
XP_024303946.1:p.Arg437Thr
|
|
XR_002957015.1:n.3296G>C
|
|
|
NM_025145.7:c.3410G>C
MANE Select
|
NP_079421.5:p.Arg1137Thr
|
|