ENST00000378585.7:c.133G>T
MANE Select
|
ENSP00000367848.4:p.Asp45Tyr
|
|
ENST00000638411.1:c.133G>T
|
ENSP00000491632.1:p.Asp45Tyr
|
|
ENST00000638604.1:n.197G>T
|
|
|
ENST00000638771.1:c.133G>T
|
ENSP00000492435.1:p.Asp45Tyr
|
|
ENST00000639045.1:c.*119G>T
|
ENSP00000491997.1:n.*119G>T
|
|
ENST00000639777.1:n.737G>T
|
|
|
ENST00000639935.1:n.170G>T
|
|
|
ENST00000640030.1:c.73G>T
|
ENSP00000491411.1:p.Asp25Tyr
|
|
ENST00000640067.1:c.133G>T
|
ENSP00000491844.1:p.Asp45Tyr
|
|
ENST00000640423.1:n.142G>T
|
|
|
ENST00000640949.1:c.133G>T
|
ENSP00000492500.1:p.Asp45Tyr
|
|
ENST00000378585.5:c.133G>T
|
ENSP00000367848.4:p.Asp45Tyr
|
|
NM_000815.4:c.133G>T
|
NP_000806.2:p.Asp45Tyr
|
|
XM_011541194.1:c.172G>T
|
XP_011539496.1:p.Asp58Tyr
|
|
XM_011541194.3:c.172G>T
|
XP_011539496.1:p.Asp58Tyr
|
|
XM_017000936.1:c.838G>T
|
XP_016856425.1:p.Asp280Tyr
|
|
NM_000815.5:c.133G>T
MANE Select
|
NP_000806.2:p.Asp45Tyr
|
|