ENST00000233190.11:c.1741G>T
MANE Select
|
ENSP00000233190.5:p.Asp581Tyr
|
|
ENST00000233190.10:c.1741G>T
|
ENSP00000233190.5:p.Asp581Tyr
|
|
ENST00000423725.5:c.1570G>T
|
ENSP00000397760.1:p.Asp524Tyr
|
|
ENST00000432169.5:c.1408G>T
|
ENSP00000409689.1:p.Asp470Tyr
|
|
ENST00000440274.5:c.1633G>T
|
ENSP00000409766.1:p.Asp545Tyr
|
|
ENST00000449699.5:c.1741G>T
|
ENSP00000399912.1:p.Asp581Tyr
|
|
ENST00000455934.6:c.1783G>T
|
ENSP00000392709.2:p.Asp595Tyr
|
|
ENST00000457011.5:c.1393G>T
|
ENSP00000400976.1:p.Asp465Tyr
|
|
ENST00000498520.1:n.213G>T
|
|
|
NM_001199981.1:c.1633G>T
|
NP_001186910.1:p.Asp545Tyr
|
|
NM_001199982.1:c.1408G>T
|
NP_001186911.1:p.Asp470Tyr
|
|
NM_001199983.1:c.1570G>T
|
NP_001186912.1:p.Asp524Tyr
|
|
NM_001199984.1:c.1783G>T
|
NP_001186913.1:p.Asp595Tyr
|
|
NM_005006.6:c.1741G>T
|
NP_004997.4:p.Asp581Tyr
|
|
XM_017004188.2:c.982G>T
|
XP_016859677.1:p.Asp328Tyr
|
|
NM_001199981.2:c.1633G>T
|
NP_001186910.1:p.Asp545Tyr
|
|
NM_001199982.2:c.1408G>T
|
NP_001186911.1:p.Asp470Tyr
|
|
NM_001199983.2:c.1570G>T
|
NP_001186912.1:p.Asp524Tyr
|
|
NM_005006.7:c.1741G>T
MANE Select
|
NP_004997.4:p.Asp581Tyr
|
|
NM_001199984.2:c.1783G>T
|
NP_001186913.1:p.Asp595Tyr
|
|