ENST00000442544.7:c.1839_1840dup
MANE Select
|
ENSP00000389140.2:p.Thr614LysfsTer?
|
|
ENST00000304775.12:c.1640_1641dup
|
|
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ENST00000412726.5:c.1770_1771dup
|
ENSP00000397322.2:p.Thr591LysfsTer?
|
|
ENST00000442544.6:c.1839_1840dup
|
ENSP00000389140.2:p.Thr614LysfsTer?
|
|
ENST00000581580.5:c.804_805dup
|
ENSP00000464582.1:p.Thr269LysfsTer?
|
|
NM_005215.3:c.1839_1840dup
|
NP_005206.2:p.Thr614LysfsTer?
|
|
XM_011525843.1:c.1839_1840dup
|
XP_011524145.1:p.Thr614LysfsTer?
|
|
XM_011525844.1:c.804_805dup
|
XP_011524146.1:p.Thr269LysfsTer?
|
|
XM_011525845.1:c.1839_1840dup
|
XP_011524147.1:p.Thr614LysfsTer?
|
|
XM_011525846.1:c.1839_1840dup
|
XP_011524148.1:p.Thr614LysfsTer?
|
|
XM_011525844.2:c.804_805dup
|
XP_011524146.1:p.Thr269LysfsTer?
|
|
XM_017025568.1:c.1839_1840dup
|
XP_016881057.1:p.Thr614LysfsTer?
|
|
XM_017025569.1:c.1839_1840dup
|
XP_016881058.1:p.Thr614LysfsTer?
|
|
XM_017025570.1:c.804_805dup
|
XP_016881059.1:p.Thr269LysfsTer?
|
|
NM_005215.4:c.1839_1840dup
MANE Select
|
NP_005206.2:p.Thr614LysfsTer?
|
|