|
ENST00000696138.1:c.7055A>T
|
ENSP00000512431.1:p.Glu2352Val
|
|
|
ENST00000684826.1:c.1637A>T
|
ENSP00000509994.1:p.Glu546Val
|
|
|
ENST00000687027.1:c.1229A>T
|
ENSP00000508715.1:p.Glu410Val
|
|
|
ENST00000687863.1:n.3718A>T
|
|
|
|
ENST00000689464.1:c.12A>T
|
|
|
|
ENST00000691014.1:c.7103A>T
|
ENSP00000510595.1:p.Glu2368Val
|
|
|
ENST00000693617.1:c.1637A>T
|
ENSP00000510031.1:p.Glu546Val
|
|
|
ENST00000358273.9:c.7073A>T
MANE Select
|
ENSP00000351015.4:p.Glu2358Val
|
|
|
ENST00000356175.7:c.7010A>T
|
ENSP00000348498.3:p.Glu2337Val
|
|
|
ENST00000358273.8:c.7073A>T
|
ENSP00000351015.4:p.Glu2358Val
|
|
|
ENST00000456735.6:c.6008A>T
|
ENSP00000389907.2:p.Glu2003Val
|
|
|
ENST00000471572.6:c.456A>T
|
|
|
|
ENST00000579081.5:c.7209A>T
|
ENSP00000462408.1:n.7209A>T
|
|
|
ENST00000581790.5:c.216A>T
|
|
|
|
ENST00000582892.1:n.315A>T
|
|
|
|
ENST00000584328.1:n.487A>T
|
|
|
|
NM_000267.3:c.7010A>T , LRG_214t1:c.7010A>T
|
NP_000258.1:p.Glu2337Val
|
|
|
NM_001042492.2:c.7073A>T , LRG_214t2:c.7073A>T
|
NP_001035957.1:p.Glu2358Val
|
|
|
XM_005257983.1:c.7073A>T
|
XP_005258040.1:p.Glu2358Val
|
|
|
XM_005257984.1:c.7010A>T
|
XP_005258041.1:p.Glu2337Val
|
|
|
XM_006721922.1:c.7103A>T
|
XP_006721985.1:p.Glu2368Val
|
|
|
XM_006721923.2:c.7064A>T
|
XP_006721986.1:p.Glu2355Val
|
|
|
XM_006721924.1:c.7103A>T
|
XP_006721987.1:p.Glu2368Val
|
|
|
XM_006721925.1:c.7040A>T
|
XP_006721988.1:p.Glu2347Val
|
|
|
XM_006721926.2:c.7103A>T
|
XP_006721989.1:p.Glu2368Val
|
|
|
XM_006721927.1:c.7103A>T
|
XP_006721990.1:p.Glu2368Val
|
|
|
XM_011524852.1:c.7100A>T
|
XP_011523154.1:p.Glu2367Val
|
|
|
XM_011524853.1:c.7064A>T
|
XP_011523155.1:p.Glu2355Val
|
|
|
XM_011524854.1:c.7064A>T
|
XP_011523156.1:p.Glu2355Val
|
|
|
XM_011524855.1:c.7064A>T
|
XP_011523157.1:p.Glu2355Val
|
|
|
XM_011524856.1:c.7064A>T
|
XP_011523158.1:p.Glu2355Val
|
|
|
XM_011524857.1:c.7103A>T
|
XP_011523159.1:p.Glu2368Val
|
|
|
NM_001042492.3:c.7073A>T
MANE Select
|
NP_001035957.1:p.Glu2358Val
|
|
