ENST00000436784.7:c.1495G>T
MANE Select
|
ENSP00000389175.2:p.Gly499Trp
|
|
ENST00000436784.6:c.1495G>T
|
ENSP00000389175.2:p.Gly499Trp
|
|
ENST00000461183.5:c.767G>T
|
ENSP00000417264.1:p.Trp256Leu
|
|
ENST00000471180.5:c.638G>T
|
ENSP00000417526.1:p.Trp213Leu
|
|
ENST00000473032.5:c.533G>T
|
ENSP00000418951.1:p.Trp178Leu
|
|
ENST00000486393.5:c.*858G>T
|
ENSP00000419868.1:n.*858G>T
|
|
ENST00000489173.1:n.1789G>T
|
|
|
NM_145262.3:c.1495G>T
|
NP_660305.2:p.Gly499Trp
|
|
NR_026699.1:n.1593G>T
|
|
|
NR_026700.1:n.699G>T
|
|
|
NR_026701.1:n.1591G>T
|
|
|
NR_026702.1:n.629G>T
|
|
|
XM_005264878.2:c.*614G>T
|
XP_005264935.1:n.*614G>T
|
|
XR_245095.2:n.2746G>T
|
|
|
XM_017005730.1:c.1114G>T
|
XP_016861219.1:p.Gly372Trp
|
|
XM_024453351.1:c.1495G>T
|
XP_024309119.1:p.Gly499Trp
|
|
XM_024453352.1:c.*614G>T
|
XP_024309120.1:n.*614G>T
|
|
XR_001740022.2:n.3397G>T
|
|
|
XR_001740023.2:n.2921G>T
|
|
|
XR_245095.4:n.2747G>T
|
|
|
NM_145262.4:c.1495G>T
MANE Select
|
NP_660305.2:p.Gly499Trp
|
|
NR_026699.2:n.1585G>T
|
|
|
NR_026700.2:n.691G>T
|
|
|
NR_026701.2:n.1583G>T
|
|
|
NR_026702.2:n.621G>T
|
|
|
NM_001144951.2:c.*614G>T
|
NP_001138423.1:n.*614G>T
|
|