ENST00000436784.7:c.1500A=
MANE Select
|
ENSP00000389175.2:p.Ala500=
|
|
ENST00000436784.6:c.1500A=
|
ENSP00000389175.2:p.Ala500=
|
|
ENST00000461183.5:c.772A=
|
ENSP00000417264.1:p.Thr258=
|
|
ENST00000471180.5:c.643A=
|
ENSP00000417526.1:p.Thr215=
|
|
ENST00000473032.5:c.538A=
|
ENSP00000418951.1:p.Thr180=
|
|
ENST00000486393.5:c.*863A=
|
ENSP00000419868.1:n.*863A=
|
|
ENST00000489173.1:n.1794A=
|
|
|
NM_145262.3:c.1500A=
|
NP_660305.2:p.Ala500=
|
|
NR_026699.1:n.1598A=
|
|
|
NR_026700.1:n.704A=
|
|
|
NR_026701.1:n.1596A=
|
|
|
NR_026702.1:n.634A=
|
|
|
XM_005264878.2:c.*619A=
|
XP_005264935.1:n.*619A=
|
|
XR_245095.2:n.2751A=
|
|
|
XM_017005730.1:c.1119A=
|
XP_016861219.1:p.Ala373=
|
|
XM_024453351.1:c.1500A=
|
XP_024309119.1:p.Ala500=
|
|
XM_024453352.1:c.*619A=
|
XP_024309120.1:n.*619A=
|
|
XR_001740022.2:n.3402A=
|
|
|
XR_001740023.2:n.2926A=
|
|
|
XR_245095.4:n.2752A=
|
|
|
NM_145262.4:c.1500A=
MANE Select
|
NP_660305.2:p.Ala500=
|
|
NR_026699.2:n.1590A=
|
|
|
NR_026700.2:n.696A=
|
|
|
NR_026701.2:n.1588A=
|
|
|
NR_026702.2:n.626A=
|
|
|
NM_001144951.2:c.*619A=
|
NP_001138423.1:n.*619A=
|
|