ENST00000436784.7:c.1527T=
MANE Select
|
ENSP00000389175.2:p.Gly509=
|
|
ENST00000436784.6:c.1527T=
|
ENSP00000389175.2:p.Gly509=
|
|
ENST00000461183.5:c.799T=
|
ENSP00000417264.1:p.Tyr267=
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|
ENST00000471180.5:c.670T=
|
ENSP00000417526.1:p.Tyr224=
|
|
ENST00000473032.5:c.565T=
|
ENSP00000418951.1:p.Tyr189=
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|
ENST00000486393.5:c.*890T=
|
ENSP00000419868.1:n.*890T=
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|
ENST00000489173.1:n.1821T=
|
|
|
NM_145262.3:c.1527T=
|
NP_660305.2:p.Gly509=
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|
NR_026699.1:n.1625T=
|
|
|
NR_026700.1:n.731T=
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|
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NR_026701.1:n.1623T=
|
|
|
NR_026702.1:n.661T=
|
|
|
XM_005264878.2:c.*646T=
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XP_005264935.1:n.*646T=
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|
XR_245095.2:n.2778T=
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|
|
XM_017005730.1:c.1146T=
|
XP_016861219.1:p.Gly382=
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|
XM_024453351.1:c.1527T=
|
XP_024309119.1:p.Gly509=
|
|
XM_024453352.1:c.*646T=
|
XP_024309120.1:n.*646T=
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|
XR_001740022.2:n.3429T=
|
|
|
XR_001740023.2:n.2953T=
|
|
|
XR_245095.4:n.2779T=
|
|
|
NM_145262.4:c.1527T=
MANE Select
|
NP_660305.2:p.Gly509=
|
|
NR_026699.2:n.1617T=
|
|
|
NR_026700.2:n.723T=
|
|
|
NR_026701.2:n.1615T=
|
|
|
NR_026702.2:n.653T=
|
|
|
NM_001144951.2:c.*646T=
|
NP_001138423.1:n.*646T=
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