ENST00000541562.6:c.2365G>A
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ENSP00000441000.2:p.Ala789Thr
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ENST00000672801.1:c.2359G>A
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ENSP00000500615.1:p.Ala787Thr
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ENST00000676266.1:c.2365G>A
MANE Select
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ENSP00000502585.1:p.Ala789Thr
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ENST00000321897.9:c.2365G>A
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ENSP00000316092.5:p.Ala789Thr
|
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ENST00000469358.5:n.2353G>A
|
|
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ENST00000473916.1:n.76G>A
|
|
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ENST00000476162.5:n.1152G>A
|
|
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ENST00000477052.1:n.451G>A
|
|
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ENST00000477288.5:n.4978G>A
|
|
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ENST00000541562.5:c.2455G>A
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ENSP00000441000.1:p.Ala819Thr
|
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ENST00000542001.5:c.2359G>A
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ENSP00000438200.2:p.Ala787Thr
|
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ENST00000625423.2:c.1945G>A
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ENSP00000485818.1:p.Ala649Thr
|
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NM_001167733.2:c.1945G>A
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NP_001161205.1:p.Ala649Thr
|
|
NM_001167734.1:c.2455G>A
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NP_001161206.1:p.Ala819Thr
|
|
NM_020442.5:c.2365G>A
|
NP_065175.4:p.Ala789Thr
|
|
NM_001167733.3:c.1945G>A
|
NP_001161205.1:p.Ala649Thr
|
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NM_001167734.2:c.2455G>A
|
NP_001161206.1:p.Ala819Thr
|
|
NM_020442.6:c.2365G>A
MANE Select
|
NP_065175.4:p.Ala789Thr
|
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