ENST00000695850.1:n.821A>G
|
|
|
ENST00000695851.1:n.25A>G
|
|
|
ENST00000695853.1:c.*704A>G
|
ENSP00000512218.1:n.*704A>G
|
|
ENST00000423902.7:c.7645A>G
MANE Select
|
ENSP00000392028.1:p.Ile2549Val
|
|
ENST00000423902.6:c.7645A>G
|
ENSP00000392028.1:p.Ile2549Val
|
|
ENST00000524602.5:c.1717-1289A>G
|
ENSP00000437061.1:n.1717-1289A>G
|
|
ENST00000531695.1:n.69A>G
|
|
|
ENST00000618450.1:n.37A>G
|
|
|
NM_001316690.1:c.1717-1289A>G
|
NP_001303619.1:n.1717-1289A>G
|
|
NM_017780.3:c.7645A>G
|
NP_060250.2:p.Ile2549Val
|
|
XM_011517553.1:c.7735A>G
|
XP_011515855.1:p.Ile2579Val
|
|
XM_011517554.1:c.7735A>G
|
XP_011515856.1:p.Ile2579Val
|
|
XM_011517555.1:c.7732A>G
|
XP_011515857.1:p.Ile2578Val
|
|
XM_011517556.1:c.7699-1256A>G
|
XP_011515858.1:n.7699-1256A>G
|
|
XM_011517557.1:c.5722A>G
|
XP_011515859.1:p.Ile1908Val
|
|
XM_011517558.1:c.5272A>G
|
XP_011515860.1:p.Ile1758Val
|
|
XM_011517559.1:c.4480A>G
|
XP_011515861.1:p.Ile1494Val
|
|
XM_011517553.2:c.7735A>G
|
XP_011515855.1:p.Ile2579Val
|
|
XM_011517554.3:c.7735A>G
|
XP_011515856.1:p.Ile2579Val
|
|
XM_011517555.2:c.7732A>G
|
XP_011515857.1:p.Ile2578Val
|
|
XM_017013612.1:c.7735A>G
|
XP_016869101.1:p.Ile2579Val
|
|
XM_017013613.1:c.7642A>G
|
XP_016869102.1:p.Ile2548Val
|
|
NM_017780.4:c.7645A>G
MANE Select
|
NP_060250.2:p.Ile2549Val
|
|