ENST00000233190.11:c.800C>T
MANE Select
|
ENSP00000233190.5:p.Thr267Ile
|
|
ENST00000233190.10:c.800C>T
|
ENSP00000233190.5:p.Thr267Ile
|
|
ENST00000423725.5:c.629C>T
|
ENSP00000397760.1:p.Thr210Ile
|
|
ENST00000432169.5:c.467C>T
|
ENSP00000409689.1:p.Thr156Ile
|
|
ENST00000440274.5:c.692C>T
|
ENSP00000409766.1:p.Thr231Ile
|
|
ENST00000449699.5:c.800C>T
|
ENSP00000399912.1:p.Thr267Ile
|
|
ENST00000455934.6:c.842C>T
|
ENSP00000392709.2:p.Thr281Ile
|
|
ENST00000457011.5:c.452C>T
|
ENSP00000400976.1:p.Thr151Ile
|
|
NM_001199981.1:c.692C>T
|
NP_001186910.1:p.Thr231Ile
|
|
NM_001199982.1:c.467C>T
|
NP_001186911.1:p.Thr156Ile
|
|
NM_001199983.1:c.629C>T
|
NP_001186912.1:p.Thr210Ile
|
|
NM_001199984.1:c.842C>T
|
NP_001186913.1:p.Thr281Ile
|
|
NM_005006.6:c.800C>T
|
NP_004997.4:p.Thr267Ile
|
|
XM_017004188.2:c.41C>T
|
XP_016859677.1:p.Thr14Ile
|
|
NM_001199981.2:c.692C>T
|
NP_001186910.1:p.Thr231Ile
|
|
NM_001199982.2:c.467C>T
|
NP_001186911.1:p.Thr156Ile
|
|
NM_001199983.2:c.629C>T
|
NP_001186912.1:p.Thr210Ile
|
|
NM_005006.7:c.800C>T
MANE Select
|
NP_004997.4:p.Thr267Ile
|
|
NM_001199984.2:c.842C>T
|
NP_001186913.1:p.Thr281Ile
|
|