ENST00000436784.7:c.1526G>A
MANE Select
|
ENSP00000389175.2:p.Gly509Asp
|
|
ENST00000436784.6:c.1526G>A
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ENSP00000389175.2:p.Gly509Asp
|
|
ENST00000461183.5:c.798G>A
|
ENSP00000417264.1:p.Arg266=
|
|
ENST00000471180.5:c.669G>A
|
ENSP00000417526.1:p.Arg223=
|
|
ENST00000473032.5:c.564G>A
|
ENSP00000418951.1:p.Arg188=
|
|
ENST00000486393.5:c.*889G>A
|
ENSP00000419868.1:n.*889G>A
|
|
ENST00000489173.1:n.1820G>A
|
|
|
NM_145262.3:c.1526G>A
|
NP_660305.2:p.Gly509Asp
|
|
NR_026699.1:n.1624G>A
|
|
|
NR_026700.1:n.730G>A
|
|
|
NR_026701.1:n.1622G>A
|
|
|
NR_026702.1:n.660G>A
|
|
|
XM_005264878.2:c.*645G>A
|
XP_005264935.1:n.*645G>A
|
|
XR_245095.2:n.2777G>A
|
|
|
XM_017005730.1:c.1145G>A
|
XP_016861219.1:p.Gly382Asp
|
|
XM_024453351.1:c.1526G>A
|
XP_024309119.1:p.Gly509Asp
|
|
XM_024453352.1:c.*645G>A
|
XP_024309120.1:n.*645G>A
|
|
XR_001740022.2:n.3428G>A
|
|
|
XR_001740023.2:n.2952G>A
|
|
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XR_245095.4:n.2778G>A
|
|
|
NM_145262.4:c.1526G>A
MANE Select
|
NP_660305.2:p.Gly509Asp
|
|
NR_026699.2:n.1616G>A
|
|
|
NR_026700.2:n.722G>A
|
|
|
NR_026701.2:n.1614G>A
|
|
|
NR_026702.2:n.652G>A
|
|
|
NM_001144951.2:c.*645G>A
|
NP_001138423.1:n.*645G>A
|
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