ENST00000436784.7:c.1528A=
MANE Select
|
ENSP00000389175.2:p.Thr510=
|
|
ENST00000436784.6:c.1528A=
|
ENSP00000389175.2:p.Thr510=
|
|
ENST00000461183.5:c.800A=
|
ENSP00000417264.1:p.Tyr267=
|
|
ENST00000471180.5:c.671A=
|
ENSP00000417526.1:p.Tyr224=
|
|
ENST00000473032.5:c.566A=
|
ENSP00000418951.1:p.Tyr189=
|
|
ENST00000486393.5:c.*891A=
|
ENSP00000419868.1:n.*891A=
|
|
ENST00000489173.1:n.1822A=
|
|
|
NM_145262.3:c.1528A=
|
NP_660305.2:p.Thr510=
|
|
NR_026699.1:n.1626A=
|
|
|
NR_026700.1:n.732A=
|
|
|
NR_026701.1:n.1624A=
|
|
|
NR_026702.1:n.662A=
|
|
|
XM_005264878.2:c.*647A=
|
XP_005264935.1:n.*647A=
|
|
XR_245095.2:n.2779A=
|
|
|
XM_017005730.1:c.1147A=
|
XP_016861219.1:p.Thr383=
|
|
XM_024453351.1:c.1528A=
|
XP_024309119.1:p.Thr510=
|
|
XM_024453352.1:c.*647A=
|
XP_024309120.1:n.*647A=
|
|
XR_001740022.2:n.3430A=
|
|
|
XR_001740023.2:n.2954A=
|
|
|
XR_245095.4:n.2780A=
|
|
|
NM_145262.4:c.1528A=
MANE Select
|
NP_660305.2:p.Thr510=
|
|
NR_026699.2:n.1618A=
|
|
|
NR_026700.2:n.724A=
|
|
|
NR_026701.2:n.1616A=
|
|
|
NR_026702.2:n.654A=
|
|
|
NM_001144951.2:c.*647A=
|
NP_001138423.1:n.*647A=
|
|