ENST00000403559.9:c.1642T>G
|
ENSP00000385069.4:p.Tyr548Asp
|
|
ENST00000703612.1:c.1582T>G
|
ENSP00000515396.1:p.Tyr528Asp
|
|
ENST00000703613.1:c.1642T>G
|
ENSP00000515397.1:p.Tyr548Asp
|
|
ENST00000703614.1:c.1591T>G
|
ENSP00000515398.1:p.Tyr531Asp
|
|
ENST00000703616.1:c.1717T>G
|
ENSP00000515400.1:p.Tyr573Asp
|
|
ENST00000703617.1:c.1036T>G
|
ENSP00000515401.1:p.Tyr346Asp
|
|
ENST00000703618.1:c.545-2448T>G
|
|
|
ENST00000350908.9:c.1591T>G
MANE Select
|
ENSP00000265436.7:p.Tyr531Asp
|
|
ENST00000393489.8:c.*1385T>G
|
ENSP00000377129.4:n.*1385T>G
|
|
ENST00000350908.8:c.1591T>G
|
ENSP00000265436.7:p.Tyr531Asp
|
|
ENST00000393489.7:c.1315T>G
|
ENSP00000377129.3:p.Tyr439Asp
|
|
ENST00000393491.7:c.1036T>G
|
ENSP00000377130.3:p.Tyr346Asp
|
|
ENST00000393494.6:c.1591T>G
|
ENSP00000377132.2:p.Tyr531Asp
|
|
ENST00000393498.6:c.1528T>G
|
ENSP00000377135.2:p.Tyr510Asp
|
|
ENST00000403559.8:c.1642T>G
|
ENSP00000385069.4:p.Tyr548Asp
|
|
ENST00000408937.7:c.1666T>G
|
ENSP00000386200.3:p.Tyr556Asp
|
|
ENST00000412402.5:c.*1309T>G
|
ENSP00000405470.1:n.*1309T>G
|
|
ENST00000441290.6:c.*1591T>G
|
ENSP00000416825.1:n.*1591T>G
|
|
ENST00000634411.1:c.1540T>G
|
ENSP00000489135.1:p.Tyr514Asp
|
|
ENST00000634623.1:c.1531T>G
|
ENSP00000488944.1:p.Tyr511Asp
|
|
ENST00000635109.1:c.*1388T>G
|
ENSP00000489457.1:n.*1388T>G
|
|
ENST00000635534.1:c.1582T>G
|
ENSP00000489229.1:p.Tyr528Asp
|
|
ENST00000635638.1:c.1594T>G
|
ENSP00000489073.1:p.Tyr532Asp
|
|
NM_001172766.2:c.1588T>G
|
NP_001166237.1:p.Tyr530Asp
|
|
NM_014491.3:c.1591T>G
|
NP_055306.1:p.Tyr531Asp
|
|
NM_148898.3:c.1666T>G
|
NP_683696.2:p.Tyr556Asp
|
|
NM_148900.3:c.1642T>G
|
NP_683698.2:p.Tyr548Asp
|
|
NR_033766.1:n.1976T>G
|
|
|
NR_033767.1:n.2023T>G
|
|
|
XM_011516706.1:c.1735T>G
|
XP_011515008.1:p.Tyr579Asp
|
|
XM_017012801.2:c.1666T>G
|
XP_016868290.1:p.Tyr556Asp
|
|
NM_014491.4:c.1591T>G
MANE Select
|
NP_055306.1:p.Tyr531Asp
|
|
NM_001172766.3:c.1588T>G
|
NP_001166237.1:p.Tyr530Asp
|
|
NM_148898.4:c.1666T>G
|
NP_683696.2:p.Tyr556Asp
|
|
NR_033766.2:n.1959T>G
|
|
|
NR_033767.2:n.2205T>G
|
|
|
NM_148900.4:c.1642T>G
|
NP_683698.2:p.Tyr548Asp
|
|