ENST00000436784.7:c.1503C>G
MANE Select
|
ENSP00000389175.2:p.His501Gln
|
|
ENST00000436784.6:c.1503C>G
|
ENSP00000389175.2:p.His501Gln
|
|
ENST00000461183.5:c.775C>G
|
ENSP00000417264.1:p.Pro259Ala
|
|
ENST00000471180.5:c.646C>G
|
ENSP00000417526.1:p.Pro216Ala
|
|
ENST00000473032.5:c.541C>G
|
ENSP00000418951.1:p.Pro181Ala
|
|
ENST00000486393.5:c.*866C>G
|
ENSP00000419868.1:n.*866C>G
|
|
ENST00000489173.1:n.1797C>G
|
|
|
NM_145262.3:c.1503C>G
|
NP_660305.2:p.His501Gln
|
|
NR_026699.1:n.1601C>G
|
|
|
NR_026700.1:n.707C>G
|
|
|
NR_026701.1:n.1599C>G
|
|
|
NR_026702.1:n.637C>G
|
|
|
XM_005264878.2:c.*622C>G
|
XP_005264935.1:n.*622C>G
|
|
XR_245095.2:n.2754C>G
|
|
|
XM_017005730.1:c.1122C>G
|
XP_016861219.1:p.His374Gln
|
|
XM_024453351.1:c.1503C>G
|
XP_024309119.1:p.His501Gln
|
|
XM_024453352.1:c.*622C>G
|
XP_024309120.1:n.*622C>G
|
|
XR_001740022.2:n.3405C>G
|
|
|
XR_001740023.2:n.2929C>G
|
|
|
XR_245095.4:n.2755C>G
|
|
|
NM_145262.4:c.1503C>G
MANE Select
|
NP_660305.2:p.His501Gln
|
|
NR_026699.2:n.1593C>G
|
|
|
NR_026700.2:n.699C>G
|
|
|
NR_026701.2:n.1591C>G
|
|
|
NR_026702.2:n.629C>G
|
|
|
NM_001144951.2:c.*622C>G
|
NP_001138423.1:n.*622C>G
|
|