ENST00000436784.7:c.1515A>G
MANE Select
|
ENSP00000389175.2:p.Thr505=
|
|
ENST00000436784.6:c.1515A>G
|
ENSP00000389175.2:p.Thr505=
|
|
ENST00000461183.5:c.787A>G
|
ENSP00000417264.1:p.Arg263Gly
|
|
ENST00000471180.5:c.658A>G
|
ENSP00000417526.1:p.Arg220Gly
|
|
ENST00000473032.5:c.553A>G
|
ENSP00000418951.1:p.Arg185Gly
|
|
ENST00000486393.5:c.*878A>G
|
ENSP00000419868.1:n.*878A>G
|
|
ENST00000489173.1:n.1809A>G
|
|
|
NM_145262.3:c.1515A>G
|
NP_660305.2:p.Thr505=
|
|
NR_026699.1:n.1613A>G
|
|
|
NR_026700.1:n.719A>G
|
|
|
NR_026701.1:n.1611A>G
|
|
|
NR_026702.1:n.649A>G
|
|
|
XM_005264878.2:c.*634A>G
|
XP_005264935.1:n.*634A>G
|
|
XR_245095.2:n.2766A>G
|
|
|
XM_017005730.1:c.1134A>G
|
XP_016861219.1:p.Thr378=
|
|
XM_024453351.1:c.1515A>G
|
XP_024309119.1:p.Thr505=
|
|
XM_024453352.1:c.*634A>G
|
XP_024309120.1:n.*634A>G
|
|
XR_001740022.2:n.3417A>G
|
|
|
XR_001740023.2:n.2941A>G
|
|
|
XR_245095.4:n.2767A>G
|
|
|
NM_145262.4:c.1515A>G
MANE Select
|
NP_660305.2:p.Thr505=
|
|
NR_026699.2:n.1605A>G
|
|
|
NR_026700.2:n.711A>G
|
|
|
NR_026701.2:n.1603A>G
|
|
|
NR_026702.2:n.641A>G
|
|
|
NM_001144951.2:c.*634A>G
|
NP_001138423.1:n.*634A>G
|
|