ENST00000295497.13:c.925G>A
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ENSP00000295497.7:p.Ala309Thr
|
|
ENST00000295497.12:c.925G>A
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ENSP00000295497.7:p.Ala309Thr
|
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ENST00000409900.9:c.1300G>A
MANE Select
|
ENSP00000386741.4:p.Ala434Thr
|
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ENST00000413882.6:c.754G>A
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ENSP00000410496.2:p.Ala252Thr
|
|
ENST00000443238.6:c.778G>A
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ENSP00000409798.2:p.Ala260Thr
|
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ENST00000488080.6:n.943G>A
|
|
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ENST00000650731.1:c.625G>A
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ENSP00000499146.1:p.Ala209Thr
|
|
ENST00000650938.1:c.686G>A
|
|
|
ENST00000651246.1:c.892G>A
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ENSP00000498484.1:p.Ala298Thr
|
|
ENST00000651501.1:c.*747G>A
|
ENSP00000498894.1:n.*747G>A
|
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ENST00000651717.1:c.*576G>A
|
ENSP00000499124.1:n.*576G>A
|
|
ENST00000652036.1:c.976G>A
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ENSP00000499139.1:p.Ala326Thr
|
|
ENST00000295497.11:c.925G>A
|
ENSP00000295497.7:p.Ala309Thr
|
|
ENST00000409156.7:c.1222G>A
|
ENSP00000386470.3:p.Ala408Thr
|
|
ENST00000409597.5:c.748G>A
|
ENSP00000386469.1:p.Ala250Thr
|
|
ENST00000409900.7:c.1300G>A
|
ENSP00000386741.3:p.Ala434Thr
|
|
ENST00000488080.5:n.1151G>A
|
|
|
ENST00000492964.1:n.443G>A
|
|
|
NM_001025201.3:c.1222G>A
|
NP_001020372.2:p.Ala408Thr
|
|
NM_001206602.1:c.925G>A
|
NP_001193531.1:p.Ala309Thr
|
|
NM_001822.5:c.1300G>A
|
NP_001813.1:p.Ala434Thr
|
|
NR_038133.1:n.1166G>A
|
|
|
NM_001025201.4:c.1222G>A
|
NP_001020372.2:p.Ala408Thr
|
|
NM_001206602.2:c.925G>A
|
NP_001193531.1:p.Ala309Thr
|
|
NM_001371513.1:c.1300G>A
|
NP_001358442.1:p.Ala434Thr
|
|
NM_001371514.1:c.1351G>A
|
NP_001358443.1:p.Ala451Thr
|
|
NM_001822.7:c.1300G>A
MANE Select
|
NP_001813.1:p.Ala434Thr
|
|
NR_038133.2:n.1168G>A
|
|
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