|
ENST00000394464.7:c.1922A>T
MANE Select
|
ENSP00000377977.2:p.Asp641Val
|
|
|
ENST00000652686.1:c.1829A>T
|
ENSP00000498663.1:p.Asp610Val
|
|
|
ENST00000231509.7:c.1925A>T
|
ENSP00000231509.3:p.Asp642Val
|
|
|
ENST00000343796.6:c.1922A>T
|
ENSP00000343205.2:p.Asp641Val
|
|
|
ENST00000394464.6:c.1922A>T
|
ENSP00000377977.2:p.Asp641Val
|
|
|
ENST00000394466.6:c.1925A>T
|
ENSP00000377979.2:p.Asp642Val
|
|
|
ENST00000415690.6:c.1922A>T
|
ENSP00000387672.2:p.Asp641Val
|
|
|
ENST00000424646.6:c.1844A>T
|
ENSP00000405282.2:p.Asp615Val
|
|
|
ENST00000503201.1:c.1922A>T
|
ENSP00000427672.1:p.Asp641Val
|
|
|
ENST00000504572.5:c.1925A>T
|
ENSP00000422518.1:p.Asp642Val
|
|
|
NM_000176.2:c.1922A>T
|
NP_000167.1:p.Asp641Val
|
|
|
NM_001018074.1:c.1922A>T
|
NP_001018084.1:p.Asp641Val
|
|
|
NM_001018075.1:c.1922A>T
|
NP_001018085.1:p.Asp641Val
|
|
|
NM_001018076.1:c.1922A>T
|
NP_001018086.1:p.Asp641Val
|
|
|
NM_001018077.1:c.1922A>T
|
NP_001018087.1:p.Asp641Val
|
|
|
NM_001020825.1:c.1922A>T
|
NP_001018661.1:p.Asp641Val
|
|
|
NM_001024094.1:c.1925A>T
|
NP_001019265.1:p.Asp642Val
|
|
|
NM_001204258.1:c.1844A>T
|
NP_001191187.1:p.Asp615Val
|
|
|
NM_001204259.1:c.1667A>T
|
NP_001191188.1:p.Asp556Val
|
|
|
NM_001204260.1:c.1655A>T
|
NP_001191189.1:p.Asp552Val
|
|
|
NM_001204261.1:c.1631A>T
|
NP_001191190.1:p.Asp544Val
|
|
|
NM_001204262.1:c.977A>T
|
NP_001191191.1:p.Asp326Val
|
|
|
NM_001204263.1:c.932A>T
|
NP_001191192.1:p.Asp311Val
|
|
|
NM_001204264.1:c.917A>T
|
NP_001191193.1:p.Asp306Val
|
|
|
NM_001204265.1:c.1922A>T
|
NP_001191194.1:p.Asp641Val
|
|
|
XM_005268419.2:c.1925A>T
|
XP_005268476.1:p.Asp642Val
|
|
|
XM_005268420.3:c.1925A>T
|
XP_005268477.1:p.Asp642Val
|
|
|
XM_005268422.2:c.1925A>T
|
XP_005268479.1:p.Asp642Val
|
|
|
XM_005268423.2:c.1925A>T
|
XP_005268480.1:p.Asp642Val
|
|
|
XM_011537637.1:c.731A>T
|
XP_011535939.1:p.Asp244Val
|
|
|
NR_157096.1:n.845A>T
|
|
|
|
XM_005268419.4:c.1925A>T
|
XP_005268476.1:p.Asp642Val
|
|
|
XM_005268420.4:c.1925A>T
|
XP_005268477.1:p.Asp642Val
|
|
|
XM_005268422.3:c.1925A>T
|
XP_005268479.1:p.Asp642Val
|
|
|
XM_005268423.3:c.1925A>T
|
XP_005268480.1:p.Asp642Val
|
|
|
XM_011537637.3:c.731A>T
|
XP_011535939.1:p.Asp244Val
|
|
|
XM_017009397.1:c.1922A>T
|
XP_016864886.1:p.Asp641Val
|
|
|
XM_017009398.1:c.1922A>T
|
XP_016864887.1:p.Asp641Val
|
|
|
NM_000176.3:c.1922A>T
MANE Select
|
NP_000167.1:p.Asp641Val
|
|
|
NM_001364180.1:c.1922A>T
|
NP_001351109.1:p.Asp641Val
|
|
|
NM_001364181.1:c.1922A>T
|
NP_001351110.1:p.Asp641Val
|
|
|
NM_001364182.1:c.1922A>T
|
NP_001351111.1:p.Asp641Val
|
|
|
NM_001364183.1:c.1925A>T
|
NP_001351112.1:p.Asp642Val
|
|
|
NM_001364184.1:c.1925A>T
|
NP_001351113.1:p.Asp642Val
|
|
|
NM_001364185.1:c.1925A>T
|
NP_001351114.1:p.Asp642Val
|
|
|
NM_001018076.2:c.1922A>T
|
NP_001018086.1:p.Asp641Val
|
|
|
NM_001020825.2:c.1922A>T
|
NP_001018661.1:p.Asp641Val
|
|
|
NM_001024094.2:c.1925A>T
|
NP_001019265.1:p.Asp642Val
|
|
|
NM_001204258.2:c.1844A>T
|
NP_001191187.1:p.Asp615Val
|
|
|
NM_001204259.2:c.1667A>T
|
NP_001191188.1:p.Asp556Val
|
|
|
NM_001204260.2:c.1655A>T
|
NP_001191189.1:p.Asp552Val
|
|
|
NM_001204261.2:c.1631A>T
|
NP_001191190.1:p.Asp544Val
|
|
|
NM_001204262.2:c.977A>T
|
NP_001191191.1:p.Asp326Val
|
|
|
NM_001204263.2:c.932A>T
|
NP_001191192.1:p.Asp311Val
|
|
|
NM_001204264.2:c.917A>T
|
NP_001191193.1:p.Asp306Val
|
|
|
NM_001204265.2:c.1922A>T
|
NP_001191194.1:p.Asp641Val
|
|
|
NM_001364180.2:c.1922A>T
|
NP_001351109.1:p.Asp641Val
|
|
|
NM_001364181.2:c.1922A>T
|
NP_001351110.1:p.Asp641Val
|
|
|
NM_001364183.2:c.1925A>T
|
NP_001351112.1:p.Asp642Val
|
|
|
NM_001364184.2:c.1925A>T
|
NP_001351113.1:p.Asp642Val
|
|
|
NR_157096.2:n.845A>T
|
|
|
