ENST00000436784.7:c.1139A>C
MANE Select
|
ENSP00000389175.2:p.Glu380Ala
|
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ENST00000305690.12:c.*258A>C
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ENSP00000301965.9:n.*258A>C
|
|
ENST00000436784.6:c.1139A>C
|
ENSP00000389175.2:p.Glu380Ala
|
|
ENST00000461183.5:c.763+124A>C
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ENSP00000417264.1:n.763+124A>C
|
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ENST00000471180.5:c.634+124A>C
|
ENSP00000417526.1:n.634+124A>C
|
|
ENST00000473032.5:c.530-353A>C
|
ENSP00000418951.1:n.530-353A>C
|
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ENST00000477382.1:c.*258A>C
|
ENSP00000419008.1:n.*258A>C
|
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ENST00000486393.5:c.*502A>C
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ENSP00000419868.1:n.*502A>C
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ENST00000489173.1:n.1433A>C
|
|
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NM_001144951.1:c.*258A>C
|
NP_001138423.1:n.*258A>C
|
|
NM_145262.3:c.1139A>C
|
NP_660305.2:p.Glu380Ala
|
|
NR_026699.1:n.1237A>C
|
|
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NR_026700.1:n.695+124A>C
|
|
|
NR_026701.1:n.1235A>C
|
|
|
NR_026702.1:n.626-353A>C
|
|
|
XM_005264878.2:c.*258A>C
|
XP_005264935.1:n.*258A>C
|
|
XR_245095.2:n.2742+124A>C
|
|
|
XM_017005730.1:c.758A>C
|
XP_016861219.1:p.Glu253Ala
|
|
XM_024453351.1:c.1139A>C
|
XP_024309119.1:p.Glu380Ala
|
|
XM_024453352.1:c.*258A>C
|
XP_024309120.1:n.*258A>C
|
|
XR_001740022.2:n.3041A>C
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|
|
XR_001740023.2:n.2917+124A>C
|
|
|
XR_245095.4:n.2743+124A>C
|
|
|
NM_145262.4:c.1139A>C
MANE Select
|
NP_660305.2:p.Glu380Ala
|
|
NR_026699.2:n.1229A>C
|
|
|
NR_026700.2:n.687+124A>C
|
|
|
NR_026701.2:n.1227A>C
|
|
|
NR_026702.2:n.618-353A>C
|
|
|
NM_001144951.2:c.*258A>C
|
NP_001138423.1:n.*258A>C
|
|