ENST00000233190.11:c.1800G>T
MANE Select
|
ENSP00000233190.5:p.Glu600Asp
|
|
ENST00000233190.10:c.1800G>T
|
ENSP00000233190.5:p.Glu600Asp
|
|
ENST00000423725.5:c.1629G>T
|
ENSP00000397760.1:p.Glu543Asp
|
|
ENST00000432169.5:c.1467G>T
|
ENSP00000409689.1:p.Glu489Asp
|
|
ENST00000440274.5:c.1692G>T
|
ENSP00000409766.1:p.Glu564Asp
|
|
ENST00000449699.5:c.1800G>T
|
ENSP00000399912.1:p.Glu600Asp
|
|
ENST00000455934.6:c.1842G>T
|
ENSP00000392709.2:p.Glu614Asp
|
|
ENST00000457011.5:c.1452G>T
|
ENSP00000400976.1:p.Glu484Asp
|
|
ENST00000498520.1:n.272G>T
|
|
|
NM_001199981.1:c.1692G>T
|
NP_001186910.1:p.Glu564Asp
|
|
NM_001199982.1:c.1467G>T
|
NP_001186911.1:p.Glu489Asp
|
|
NM_001199983.1:c.1629G>T
|
NP_001186912.1:p.Glu543Asp
|
|
NM_001199984.1:c.1842G>T
|
NP_001186913.1:p.Glu614Asp
|
|
NM_005006.6:c.1800G>T
|
NP_004997.4:p.Glu600Asp
|
|
XM_017004188.2:c.1041G>T
|
XP_016859677.1:p.Glu347Asp
|
|
NM_001199981.2:c.1692G>T
|
NP_001186910.1:p.Glu564Asp
|
|
NM_001199982.2:c.1467G>T
|
NP_001186911.1:p.Glu489Asp
|
|
NM_001199983.2:c.1629G>T
|
NP_001186912.1:p.Glu543Asp
|
|
NM_005006.7:c.1800G>T
MANE Select
|
NP_004997.4:p.Glu600Asp
|
|
NM_001199984.2:c.1842G>T
|
NP_001186913.1:p.Glu614Asp
|
|