ENST00000233190.11:c.835G>C
MANE Select
|
ENSP00000233190.5:p.Glu279Gln
|
|
ENST00000233190.10:c.835G>C
|
ENSP00000233190.5:p.Glu279Gln
|
|
ENST00000423725.5:c.664G>C
|
ENSP00000397760.1:p.Glu222Gln
|
|
ENST00000432169.5:c.502G>C
|
ENSP00000409689.1:p.Glu168Gln
|
|
ENST00000440274.5:c.727G>C
|
ENSP00000409766.1:p.Glu243Gln
|
|
ENST00000449699.5:c.835G>C
|
ENSP00000399912.1:p.Glu279Gln
|
|
ENST00000455934.6:c.877G>C
|
ENSP00000392709.2:p.Glu293Gln
|
|
ENST00000457011.5:c.487G>C
|
ENSP00000400976.1:p.Glu163Gln
|
|
NM_001199981.1:c.727G>C
|
NP_001186910.1:p.Glu243Gln
|
|
NM_001199982.1:c.502G>C
|
NP_001186911.1:p.Glu168Gln
|
|
NM_001199983.1:c.664G>C
|
NP_001186912.1:p.Glu222Gln
|
|
NM_001199984.1:c.877G>C
|
NP_001186913.1:p.Glu293Gln
|
|
NM_005006.6:c.835G>C
|
NP_004997.4:p.Glu279Gln
|
|
XM_017004188.2:c.76G>C
|
XP_016859677.1:p.Glu26Gln
|
|
NM_001199981.2:c.727G>C
|
NP_001186910.1:p.Glu243Gln
|
|
NM_001199982.2:c.502G>C
|
NP_001186911.1:p.Glu168Gln
|
|
NM_001199983.2:c.664G>C
|
NP_001186912.1:p.Glu222Gln
|
|
NM_005006.7:c.835G>C
MANE Select
|
NP_004997.4:p.Glu279Gln
|
|
NM_001199984.2:c.877G>C
|
NP_001186913.1:p.Glu293Gln
|
|