ENST00000323130.8:c.2485C>T
|
ENSP00000314488.4:p.Gln829Ter
|
|
ENST00000409623.8:c.2440C>T
|
ENSP00000386966.4:p.Gln814Ter
|
|
ENST00000452276.6:c.2368C>T
|
ENSP00000388671.2:p.Gln790Ter
|
|
ENST00000453906.6:c.1603C>T
|
ENSP00000403035.2:p.Gln535Ter
|
|
ENST00000518896.2:c.776C>T
|
ENSP00000507992.1:n.776C>T
|
|
ENST00000520680.2:c.2608C>T
|
ENSP00000428785.2:p.Gln870Ter
|
|
ENST00000521517.6:c.2386C>T
|
ENSP00000430740.2:p.Gln796Ter
|
|
ENST00000681998.1:c.2306C>T
|
ENSP00000506773.1:n.2306C>T
|
|
ENST00000682036.1:c.1726C>T
|
ENSP00000508390.1:p.Gln576Ter
|
|
ENST00000682577.1:c.2258C>T
|
ENSP00000506963.1:n.2258C>T
|
|
ENST00000682624.1:c.*2059C>T
|
ENSP00000508343.1:n.*2059C>T
|
|
ENST00000682700.1:c.2485C>T
|
ENSP00000507627.1:p.Gln829Ter
|
|
ENST00000682744.1:n.2023C>T
|
|
|
ENST00000682804.1:n.2308C>T
|
|
|
ENST00000682837.1:c.1974C>T
|
ENSP00000507920.1:n.1974C>T
|
|
ENST00000682935.1:n.4535C>T
|
|
|
ENST00000682984.1:c.2146C>T
|
ENSP00000507209.1:p.Gln716Ter
|
|
ENST00000683078.1:c.2240C>T
|
ENSP00000506796.1:n.2240C>T
|
|
ENST00000683223.1:c.2217C>T
|
ENSP00000507685.1:n.2217C>T
|
|
ENST00000683238.1:n.3709C>T
|
|
|
ENST00000683249.1:n.4082C>T
|
|
|
ENST00000683336.1:c.2306C>T
|
ENSP00000507695.1:n.2306C>T
|
|
ENST00000683362.1:c.2146C>T
|
ENSP00000506985.1:p.Gln716Ter
|
|
ENST00000683850.1:n.2408C>T
|
|
|
ENST00000683919.1:c.2415C>T
|
ENSP00000507617.1:n.2415C>T
|
|
ENST00000683953.1:c.2396C>T
|
ENSP00000508375.1:n.2396C>T
|
|
ENST00000684023.1:c.2462C>T
|
ENSP00000507461.1:n.2462C>T
|
|
ENST00000684064.1:c.2176C>T
|
ENSP00000508192.1:p.Gln726Ter
|
|
ENST00000684089.1:n.4035C>T
|
|
|
ENST00000684149.1:c.*1664C>T
|
ENSP00000507943.1:n.*1664C>T
|
|
ENST00000684343.1:c.682C>T
|
ENSP00000507591.1:p.Gln228Ter
|
|
ENST00000684416.1:n.2444C>T
|
|
|
ENST00000684540.1:c.2415C>T
|
ENSP00000507987.1:n.2415C>T
|
|
ENST00000453321.8:c.2485C>T
MANE Select
|
ENSP00000389998.3:p.Gln829Ter
|
|
ENST00000323130.7:c.2455C>T
|
ENSP00000314488.3:p.Gln819Ter
|
|
ENST00000409623.7:c.2242C>T
|
ENSP00000386966.3:p.Gln748Ter
|
|
ENST00000453321.7:c.2485C>T
|
ENSP00000389998.3:p.Gln829Ter
|
|
ENST00000474944.5:n.1623C>T
|
|
|
ENST00000519845.5:n.1217C>T
|
|
|
NM_001142301.1:c.2242C>T , LRG_688t2:c.2242C>T
|
NP_001135773.1:p.Gln748Ter
|
|
NM_153704.5:c.2485C>T , LRG_688t1:c.2485C>T
|
NP_714915.3:p.Gln829Ter
|
|
NR_024522.1:n.2556C>T
|
|
|
XM_006716686.2:c.2182C>T
|
XP_006716749.1:p.Gln728Ter
|
|
XM_006716687.2:c.1885C>T
|
XP_006716750.1:p.Gln629Ter
|
|
XM_011517363.1:c.1603C>T
|
XP_011515665.1:p.Gln535Ter
|
|
XR_428387.1:n.2543C>T
|
|
|
XR_928360.1:n.2543C>T
|
|
|
XR_928361.1:n.2543C>T
|
|
|
XR_928362.1:n.2543C>T
|
|
|
XM_006716686.4:c.2182C>T
|
XP_006716749.1:p.Gln728Ter
|
|
XM_011517363.3:c.1603C>T
|
XP_011515665.1:p.Gln535Ter
|
|
XM_024447326.1:c.1831C>T
|
XP_024303094.1:p.Gln611Ter
|
|
XR_001745619.2:n.2526C>T
|
|
|
XR_428387.2:n.2526C>T
|
|
|
XR_928360.3:n.2526C>T
|
|
|
XR_928362.3:n.2526C>T
|
|
|
NM_153704.6:c.2485C>T
MANE Select
|
NP_714915.3:p.Gln829Ter
|
|
NR_024522.2:n.2506C>T
|
|
|