ENST00000233190.11:c.1784C>T
MANE Select
|
ENSP00000233190.5:p.Thr595Ile
|
|
ENST00000233190.10:c.1784C>T
|
ENSP00000233190.5:p.Thr595Ile
|
|
ENST00000423725.5:c.1613C>T
|
ENSP00000397760.1:p.Thr538Ile
|
|
ENST00000432169.5:c.1451C>T
|
ENSP00000409689.1:p.Thr484Ile
|
|
ENST00000440274.5:c.1676C>T
|
ENSP00000409766.1:p.Thr559Ile
|
|
ENST00000449699.5:c.1784C>T
|
ENSP00000399912.1:p.Thr595Ile
|
|
ENST00000455934.6:c.1826C>T
|
ENSP00000392709.2:p.Thr609Ile
|
|
ENST00000457011.5:c.1436C>T
|
ENSP00000400976.1:p.Thr479Ile
|
|
ENST00000498520.1:n.256C>T
|
|
|
NM_001199981.1:c.1676C>T
|
NP_001186910.1:p.Thr559Ile
|
|
NM_001199982.1:c.1451C>T
|
NP_001186911.1:p.Thr484Ile
|
|
NM_001199983.1:c.1613C>T
|
NP_001186912.1:p.Thr538Ile
|
|
NM_001199984.1:c.1826C>T
|
NP_001186913.1:p.Thr609Ile
|
|
NM_005006.6:c.1784C>T
|
NP_004997.4:p.Thr595Ile
|
|
XM_017004188.2:c.1025C>T
|
XP_016859677.1:p.Thr342Ile
|
|
NM_001199981.2:c.1676C>T
|
NP_001186910.1:p.Thr559Ile
|
|
NM_001199982.2:c.1451C>T
|
NP_001186911.1:p.Thr484Ile
|
|
NM_001199983.2:c.1613C>T
|
NP_001186912.1:p.Thr538Ile
|
|
NM_005006.7:c.1784C>T
MANE Select
|
NP_004997.4:p.Thr595Ile
|
|
NM_001199984.2:c.1826C>T
|
NP_001186913.1:p.Thr609Ile
|
|