ENST00000541682.7:c.680G>C
MANE Select
|
ENSP00000446205.2:p.Arg227Thr
|
|
ENST00000317814.8:c.665G>C
|
ENSP00000314774.4:p.Arg222Thr
|
|
ENST00000541682.6:c.680G>C
|
ENSP00000446205.2:p.Arg227Thr
|
|
NM_001165967.1:c.680G>C
|
NP_001159439.1:p.Arg227Thr
|
|
NM_032580.3:c.665G>C
|
NP_115969.2:p.Arg222Thr
|
|
XM_011524038.1:c.785G>C
|
XP_011522340.1:p.Arg262Thr
|
|
XM_011524039.1:c.776G>C
|
XP_011522341.1:p.Arg259Thr
|
|
XM_011524040.1:c.776G>C
|
XP_011522342.1:p.Arg259Thr
|
|
XM_011524041.1:c.767G>C
|
XP_011522343.1:p.Arg256Thr
|
|
XM_011524042.1:c.638G>C
|
XP_011522344.1:p.Arg213Thr
|
|
XR_934203.1:n.69+1770C>G
|
|
|
XM_017025232.1:c.785G>C
|
XP_016880721.1:p.Arg262Thr
|
|
XM_024451007.1:c.785G>C
|
XP_024306775.1:p.Arg262Thr
|
|
NM_001165967.2:c.680G>C
MANE Select
|
NP_001159439.1:p.Arg227Thr
|
|
NM_032580.4:c.665G>C
|
NP_115969.2:p.Arg222Thr
|
|