ENST00000426333.7:c.2092G>C
MANE Select
|
ENSP00000392094.1:p.Glu698Gln
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|
ENST00000402521.7:c.1987G>C
|
ENSP00000385873.2:p.Glu663Gln
|
|
ENST00000426333.6:c.2092G>C
|
ENSP00000392094.1:p.Glu698Gln
|
|
ENST00000586276.5:n.1754G>C
|
|
|
ENST00000590124.5:c.94G>C
|
ENSP00000467249.1:p.Glu32Gln
|
|
ENST00000590367.5:n.1820G>C
|
|
|
ENST00000590977.5:n.700G>C
|
|
|
ENST00000591382.5:c.2092G>C
|
ENSP00000467805.1:p.Glu698Gln
|
|
ENST00000592576.5:c.2062G>C
|
ENSP00000465058.1:p.Glu688Gln
|
|
NM_001142605.1:c.1987G>C
|
NP_001136077.1:p.Glu663Gln
|
|
NM_001258353.1:c.2092G>C
|
NP_001245282.1:p.Glu698Gln
|
|
NM_001258354.1:c.2062G>C
|
NP_001245283.1:p.Glu688Gln
|
|
NM_004247.3:c.2092G>C
|
NP_004238.3:p.Glu698Gln
|
|
XR_934602.1:n.2177G>C
|
|
|
XR_934602.3:n.2173G>C
|
|
|
NM_004247.4:c.2092G>C
MANE Select
|
NP_004238.3:p.Glu698Gln
|
|
NM_001142605.2:c.1987G>C
|
NP_001136077.1:p.Glu663Gln
|
|
NM_001258353.2:c.2092G>C
|
NP_001245282.1:p.Glu698Gln
|
|
NM_001258354.2:c.2062G>C
|
NP_001245283.1:p.Glu688Gln
|
|