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Hint: Click on a member to display user logs and details! boudi124 NBB☆Pro789◇♧ 57,791 ↑ General Stats

keberuntungan, khususnya dalam menjadi member baru dan akses ke akun pro di Taiwan meningkatkan rasa puas saat meraih kemenangan

member pro789 Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24

member pro789 Pro789 1; Ser608 1; Ser807 1; Thr252 1 AA 586-615; Reactivity All reactivities pRb belongs to the pocket protein family, whose members have a pocket for the