ENST00000695850.1:n.984T>G
|
|
|
ENST00000695851.1:n.188T>G
|
|
|
ENST00000695853.1:c.*867T>G
|
ENSP00000512218.1:n.*867T>G
|
|
ENST00000423902.7:c.7808T>G
MANE Select
|
ENSP00000392028.1:p.Val2603Gly
|
|
ENST00000423902.6:c.7808T>G
|
ENSP00000392028.1:p.Val2603Gly
|
|
ENST00000524602.5:c.1717-1126T>G
|
ENSP00000437061.1:n.1717-1126T>G
|
|
ENST00000531695.1:n.232T>G
|
|
|
ENST00000618450.1:n.200T>G
|
|
|
NM_001316690.1:c.1717-1126T>G
|
NP_001303619.1:n.1717-1126T>G
|
|
NM_017780.3:c.7808T>G
|
NP_060250.2:p.Val2603Gly
|
|
XM_011517553.1:c.7898T>G
|
XP_011515855.1:p.Val2633Gly
|
|
XM_011517554.1:c.7898T>G
|
XP_011515856.1:p.Val2633Gly
|
|
XM_011517555.1:c.7895T>G
|
XP_011515857.1:p.Val2632Gly
|
|
XM_011517556.1:c.7699-1093T>G
|
XP_011515858.1:n.7699-1093T>G
|
|
XM_011517557.1:c.5885T>G
|
XP_011515859.1:p.Val1962Gly
|
|
XM_011517558.1:c.5435T>G
|
XP_011515860.1:p.Val1812Gly
|
|
XM_011517559.1:c.4643T>G
|
XP_011515861.1:p.Val1548Gly
|
|
XM_011517553.2:c.7898T>G
|
XP_011515855.1:p.Val2633Gly
|
|
XM_011517554.3:c.7898T>G
|
XP_011515856.1:p.Val2633Gly
|
|
XM_011517555.2:c.7895T>G
|
XP_011515857.1:p.Val2632Gly
|
|
XM_017013612.1:c.7898T>G
|
XP_016869101.1:p.Val2633Gly
|
|
XM_017013613.1:c.7805T>G
|
XP_016869102.1:p.Val2602Gly
|
|
NM_017780.4:c.7808T>G
MANE Select
|
NP_060250.2:p.Val2603Gly
|
|