ENST00000371757.7:c.2257T>G
MANE Select
|
ENSP00000360822.2:p.Tyr753Asp
|
|
ENST00000674572.1:c.2098T>G
|
ENSP00000501742.1:p.Tyr700Asp
|
|
ENST00000675090.1:c.2005T>G
|
ENSP00000501833.1:p.Tyr669Asp
|
|
ENST00000675399.1:c.2005T>G
|
ENSP00000501932.1:p.Tyr669Asp
|
|
ENST00000676421.1:c.2014T>G
|
ENSP00000502322.1:p.Tyr672Asp
|
|
ENST00000263604.5:c.2158T>G
|
ENSP00000263604.4:p.Tyr720Asp
|
|
ENST00000371757.6:c.2257T>G
|
ENSP00000360822.2:p.Tyr753Asp
|
|
ENST00000460750.5:c.*1867T>G
|
ENSP00000418777.1:n.*1867T>G
|
|
ENST00000486577.6:c.2140T>G
|
ENSP00000417578.3:p.Tyr714Asp
|
|
ENST00000487664.5:c.2257T>G
|
ENSP00000417851.2:p.Tyr753Asp
|
|
ENST00000488444.6:c.2200T>G
|
ENSP00000419007.3:p.Tyr734Asp
|
|
ENST00000490355.6:c.2194T>G
|
ENSP00000418003.3:p.Tyr732Asp
|
|
ENST00000490363.3:n.2076T>G
|
|
|
ENST00000491806.6:c.2200T>G
|
ENSP00000419086.3:p.Tyr734Asp
|
|
ENST00000628528.2:c.2122T>G
|
ENSP00000486374.1:p.Tyr708Asp
|
|
ENST00000630792.2:c.2092T>G
|
ENSP00000486486.1:p.Tyr698Asp
|
|
ENST00000631073.2:c.2200T>G
|
ENSP00000486130.1:p.Tyr734Asp
|
|
ENST00000631193.1:c.106T>G
|
ENSP00000486830.1:p.Tyr36Asp
|
|
NM_001272003.1:c.2122T>G
|
NP_001258932.1:p.Tyr708Asp
|
|
NM_020822.2:c.2257T>G
|
NP_065873.2:p.Tyr753Asp
|
|
XM_011518877.1:c.2392T>G
|
XP_011517179.1:p.Tyr798Asp
|
|
XM_011518878.1:c.2401T>G
|
XP_011517180.1:p.Tyr801Asp
|
|
XM_011518879.1:c.2392T>G
|
XP_011517181.1:p.Tyr798Asp
|
|
XM_011518880.1:c.2158T>G
|
XP_011517182.1:p.Tyr720Asp
|
|
XM_011518881.1:c.1747T>G
|
XP_011517183.1:p.Tyr583Asp
|
|
XM_011518877.3:c.2392T>G
|
XP_011517179.1:p.Tyr798Asp
|
|
XM_011518878.3:c.2401T>G
|
XP_011517180.1:p.Tyr801Asp
|
|
XM_011518879.3:c.2392T>G
|
XP_011517181.1:p.Tyr798Asp
|
|
XM_011518881.3:c.1747T>G
|
XP_011517183.1:p.Tyr583Asp
|
|
XM_017014931.1:c.2191T>G
|
XP_016870420.1:p.Tyr731Asp
|
|
XM_017014932.1:c.2014T>G
|
XP_016870421.1:p.Tyr672Asp
|
|
XM_017014933.1:c.1747T>G
|
XP_016870422.1:p.Tyr583Asp
|
|
XM_024447617.1:c.1747T>G
|
XP_024303385.1:p.Tyr583Asp
|
|
XM_024447618.1:c.1747T>G
|
XP_024303386.1:p.Tyr583Asp
|
|
NM_020822.3:c.2257T>G
MANE Select
|
NP_065873.2:p.Tyr753Asp
|
|
NM_001272003.2:c.2122T>G
|
NP_001258932.1:p.Tyr708Asp
|
|