ENST00000233190.11:c.754G>C
MANE Select
|
ENSP00000233190.5:p.Asp252His
|
|
ENST00000233190.10:c.754G>C
|
ENSP00000233190.5:p.Asp252His
|
|
ENST00000423725.5:c.583G>C
|
ENSP00000397760.1:p.Asp195His
|
|
ENST00000432169.5:c.421G>C
|
ENSP00000409689.1:p.Asp141His
|
|
ENST00000440274.5:c.646G>C
|
ENSP00000409766.1:p.Asp216His
|
|
ENST00000449699.5:c.754G>C
|
ENSP00000399912.1:p.Asp252His
|
|
ENST00000455934.6:c.796G>C
|
ENSP00000392709.2:p.Asp266His
|
|
ENST00000457011.5:c.406G>C
|
ENSP00000400976.1:p.Asp136His
|
|
NM_001199981.1:c.646G>C
|
NP_001186910.1:p.Asp216His
|
|
NM_001199982.1:c.421G>C
|
NP_001186911.1:p.Asp141His
|
|
NM_001199983.1:c.583G>C
|
NP_001186912.1:p.Asp195His
|
|
NM_001199984.1:c.796G>C
|
NP_001186913.1:p.Asp266His
|
|
NM_005006.6:c.754G>C
|
NP_004997.4:p.Asp252His
|
|
XM_017004188.2:c.-6G>C
|
XP_016859677.1:n.-6G>C
|
|
NM_001199981.2:c.646G>C
|
NP_001186910.1:p.Asp216His
|
|
NM_001199982.2:c.421G>C
|
NP_001186911.1:p.Asp141His
|
|
NM_001199983.2:c.583G>C
|
NP_001186912.1:p.Asp195His
|
|
NM_005006.7:c.754G>C
MANE Select
|
NP_004997.4:p.Asp252His
|
|
NM_001199984.2:c.796G>C
|
NP_001186913.1:p.Asp266His
|
|