ENST00000233190.11:c.1766A>G
MANE Select
|
ENSP00000233190.5:p.Tyr589Cys
|
|
ENST00000233190.10:c.1766A>G
|
ENSP00000233190.5:p.Tyr589Cys
|
|
ENST00000423725.5:c.1595A>G
|
ENSP00000397760.1:p.Tyr532Cys
|
|
ENST00000432169.5:c.1433A>G
|
ENSP00000409689.1:p.Tyr478Cys
|
|
ENST00000440274.5:c.1658A>G
|
ENSP00000409766.1:p.Tyr553Cys
|
|
ENST00000449699.5:c.1766A>G
|
ENSP00000399912.1:p.Tyr589Cys
|
|
ENST00000455934.6:c.1808A>G
|
ENSP00000392709.2:p.Tyr603Cys
|
|
ENST00000457011.5:c.1418A>G
|
ENSP00000400976.1:p.Tyr473Cys
|
|
ENST00000498520.1:n.238A>G
|
|
|
NM_001199981.1:c.1658A>G
|
NP_001186910.1:p.Tyr553Cys
|
|
NM_001199982.1:c.1433A>G
|
NP_001186911.1:p.Tyr478Cys
|
|
NM_001199983.1:c.1595A>G
|
NP_001186912.1:p.Tyr532Cys
|
|
NM_001199984.1:c.1808A>G
|
NP_001186913.1:p.Tyr603Cys
|
|
NM_005006.6:c.1766A>G
|
NP_004997.4:p.Tyr589Cys
|
|
XM_017004188.2:c.1007A>G
|
XP_016859677.1:p.Tyr336Cys
|
|
NM_001199981.2:c.1658A>G
|
NP_001186910.1:p.Tyr553Cys
|
|
NM_001199982.2:c.1433A>G
|
NP_001186911.1:p.Tyr478Cys
|
|
NM_001199983.2:c.1595A>G
|
NP_001186912.1:p.Tyr532Cys
|
|
NM_005006.7:c.1766A>G
MANE Select
|
NP_004997.4:p.Tyr589Cys
|
|
NM_001199984.2:c.1808A>G
|
NP_001186913.1:p.Tyr603Cys
|
|