ENST00000440460.7:c.1763C>A
MANE Select
|
ENSP00000394352.3:p.Pro588His
|
|
ENST00000440460.6:c.1763C>A
|
ENSP00000394352.3:p.Pro588His
|
|
ENST00000526500.5:n.759C>A
|
|
|
ENST00000615255.1:c.1130C>A
|
ENSP00000480808.1:p.Pro377His
|
|
ENST00000618522.4:n.1116C>A
|
|
|
NM_001037954.3:c.1763C>A
|
NP_001033043.1:p.Pro588His
|
|
NM_033425.4:c.1130C>A
|
NP_219493.1:p.Pro377His
|
|
XM_005277726.3:c.1763C>A
|
XP_005277783.1:p.Pro588His
|
|
XM_005277727.3:c.1760C>A
|
XP_005277784.1:p.Pro587His
|
|
XM_005277728.3:c.1130C>A
|
XP_005277785.1:p.Pro377His
|
|
XM_011543045.1:c.881C>A
|
XP_011541347.1:p.Pro294His
|
|
XM_011543046.1:c.875C>A
|
XP_011541348.1:p.Pro292His
|
|
XM_017018466.2:c.1760C>A
|
XP_016873955.1:p.Pro587His
|
|
XM_017018467.1:c.1760C>A
|
XP_016873956.1:p.Pro587His
|
|
XM_017018468.1:c.881C>A
|
XP_016873957.1:p.Pro294His
|
|
XM_017018469.1:c.875C>A
|
XP_016873958.1:p.Pro292His
|
|
XM_024448742.1:c.1655C>A
|
XP_024304510.1:p.Pro552His
|
|
XM_024448743.1:c.1652C>A
|
XP_024304511.1:p.Pro551His
|
|
NM_001037954.4:c.1763C>A
MANE Select
|
NP_001033043.1:p.Pro588His
|
|
NM_033425.5:c.1130C>A
|
NP_219493.1:p.Pro377His
|
|