ENST00000695850.1:n.888T>A
|
|
|
ENST00000695851.1:n.92T>A
|
|
|
ENST00000695853.1:c.*771T>A
|
ENSP00000512218.1:n.*771T>A
|
|
ENST00000423902.7:c.7712T>A
MANE Select
|
ENSP00000392028.1:p.Val2571Asp
|
|
ENST00000423902.6:c.7712T>A
|
ENSP00000392028.1:p.Val2571Asp
|
|
ENST00000524602.5:c.1717-1222T>A
|
ENSP00000437061.1:n.1717-1222T>A
|
|
ENST00000531695.1:n.136T>A
|
|
|
ENST00000618450.1:n.104T>A
|
|
|
NM_001316690.1:c.1717-1222T>A
|
NP_001303619.1:n.1717-1222T>A
|
|
NM_017780.3:c.7712T>A
|
NP_060250.2:p.Val2571Asp
|
|
XM_011517553.1:c.7802T>A
|
XP_011515855.1:p.Val2601Asp
|
|
XM_011517554.1:c.7802T>A
|
XP_011515856.1:p.Val2601Asp
|
|
XM_011517555.1:c.7799T>A
|
XP_011515857.1:p.Val2600Asp
|
|
XM_011517556.1:c.7699-1189T>A
|
XP_011515858.1:n.7699-1189T>A
|
|
XM_011517557.1:c.5789T>A
|
XP_011515859.1:p.Val1930Asp
|
|
XM_011517558.1:c.5339T>A
|
XP_011515860.1:p.Val1780Asp
|
|
XM_011517559.1:c.4547T>A
|
XP_011515861.1:p.Val1516Asp
|
|
XM_011517553.2:c.7802T>A
|
XP_011515855.1:p.Val2601Asp
|
|
XM_011517554.3:c.7802T>A
|
XP_011515856.1:p.Val2601Asp
|
|
XM_011517555.2:c.7799T>A
|
XP_011515857.1:p.Val2600Asp
|
|
XM_017013612.1:c.7802T>A
|
XP_016869101.1:p.Val2601Asp
|
|
XM_017013613.1:c.7709T>A
|
XP_016869102.1:p.Val2570Asp
|
|
NM_017780.4:c.7712T>A
MANE Select
|
NP_060250.2:p.Val2571Asp
|
|