ENST00000636168.2:c.445_454delinsACTGTCATCG
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ENSP00000490338.2:p.Thr149=
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ENST00000672640.1:c.445_454delinsACTGTCATCG
|
ENSP00000500507.1:p.Thr149=
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|
ENST00000261007.9:c.1009_1018delinsACTGTCATCG
|
ENSP00000261007.5:p.Thr337=
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ENST00000348749.9:c.934_943delinsACTGTCATCG
MANE Select
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ENSP00000261008.5:p.Thr312=
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ENST00000409219.5:c.934_943delinsACTGTCATCG
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ENSP00000386611.1:p.Thr312=
|
|
ENST00000409542.5:c.688_697delinsACTGTCATCG
|
ENSP00000387026.1:p.Thr230=
|
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ENST00000435083.5:c.*578_*587delinsACTGTCATCG
|
ENSP00000395805.1:n.*578_*587delinsACTGTCATCG
|
|
NM_000079.3:c.934_943delinsACTGTCATCG
|
NP_000070.1:p.Thr312=
|
|
NM_001039523.2:c.1009_1018delinsACTGTCATCG
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NP_001034612.1:p.Thr337=
|
|
XM_017003256.1:c.1030_1039delinsACTGTCATCG
|
XP_016858745.1:p.Thr344=
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|
XM_017003257.1:c.955_964delinsACTGTCATCG
|
XP_016858746.1:p.Thr319=
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|
NM_000079.4:c.934_943delinsACTGTCATCG
MANE Select
|
NP_000070.1:p.Thr312=
|
|
NM_001039523.3:c.1009_1018delinsACTGTCATCG
|
NP_001034612.1:p.Thr337=
|
|