|
ENST00000375687.10:c.3590C>A
MANE Select
|
ENSP00000364839.4:p.Pro1197His
|
|
|
ENST00000646985.1:c.3407C>A
|
ENSP00000495053.1:p.Pro1136His
|
|
|
ENST00000647223.1:n.5943C>A
|
|
|
|
ENST00000651418.1:c.1869+1721C>A
|
ENSP00000499150.1:n.1869+1721C>A
|
|
|
ENST00000306058.9:c.3575C>A
|
ENSP00000305119.5:p.Pro1192His
|
|
|
ENST00000375687.8:c.3590C>A
|
ENSP00000364839.4:p.Pro1197His
|
|
|
ENST00000613218.4:c.3590C>A
|
ENSP00000480487.1:p.Pro1197His
|
|
|
ENST00000620121.4:c.3590C>A
|
ENSP00000481978.1:p.Pro1197His
|
|
|
NM_015338.5:c.3590C>A , LRG_630t1:c.3590C>A
|
NP_056153.2:p.Pro1197His
|
|
|
XM_006723727.2:c.3587C>A
|
XP_006723790.1:p.Pro1196His
|
|
|
XM_006723728.2:c.3560C>A
|
XP_006723791.1:p.Pro1187His
|
|
|
XM_006723730.2:c.3506C>A
|
XP_006723793.1:p.Pro1169His
|
|
|
XM_006723732.2:c.3407C>A
|
XP_006723795.1:p.Pro1136His
|
|
|
XM_006723733.1:c.2906C>A
|
XP_006723796.1:p.Pro969His
|
|
|
XM_011528647.1:c.3854C>A
|
XP_011526949.1:p.Pro1285His
|
|
|
XM_011528648.1:c.3851C>A
|
XP_011526950.1:p.Pro1284His
|
|
|
XM_011528649.1:c.3770C>A
|
XP_011526951.1:p.Pro1257His
|
|
|
XM_011528650.1:c.3701C>A
|
XP_011526952.1:p.Pro1234His
|
|
|
XM_011528651.1:c.3569C>A
|
XP_011526953.1:p.Pro1190His
|
|
|
XM_011528652.1:c.3506C>A
|
XP_011526954.1:p.Pro1169His
|
|
|
NM_001363734.1:c.3407C>A
|
NP_001350663.1:p.Pro1136His
|
|
|
XM_006723727.3:c.3587C>A
|
XP_006723790.1:p.Pro1196His
|
|
|
XM_006723728.3:c.3560C>A
|
XP_006723791.1:p.Pro1187His
|
|
|
XM_006723730.4:c.3506C>A
|
XP_006723793.1:p.Pro1169His
|
|
|
XM_011528648.3:c.3851C>A
|
XP_011526950.1:p.Pro1284His
|
|
|
XM_011528652.2:c.3506C>A
|
XP_011526954.1:p.Pro1169His
|
|
|
XM_017027704.1:c.3506C>A
|
XP_016883193.1:p.Pro1169His
|
|
|
XM_017027705.1:c.3506C>A
|
XP_016883194.1:p.Pro1169His
|
|
|
XM_017027706.1:c.3437C>A
|
XP_016883195.1:p.Pro1146His
|
|
|
NM_015338.6:c.3590C>A
MANE Select
|
NP_056153.2:p.Pro1197His
|
|
