ENST00000682424.1:c.1550C>T
|
ENSP00000507321.1:p.Ala517Val
|
|
ENST00000299427.12:c.1664C>T
MANE Select
|
ENSP00000299427.6:p.Ala555Val
|
|
ENST00000524611.2:n.703C>T
|
|
|
ENST00000533371.6:c.935C>T
|
ENSP00000437066.1:p.Ala312Val
|
|
ENST00000642892.1:c.935C>T
|
ENSP00000494165.1:p.Ala312Val
|
|
ENST00000643342.1:c.737C>T
|
|
|
ENST00000643439.1:c.*1404C>T
|
ENSP00000495849.1:n.*1404C>T
|
|
ENST00000643479.1:n.1850C>T
|
|
|
ENST00000643516.1:c.1173C>T
|
|
|
ENST00000644218.1:c.1475C>T
|
ENSP00000493574.1:p.Ala492Val
|
|
ENST00000644683.1:c.*1117C>T
|
ENSP00000494085.1:n.*1117C>T
|
|
ENST00000644810.1:c.1385C>T
|
ENSP00000495895.1:p.Ala462Val
|
|
ENST00000644831.1:n.1840C>T
|
|
|
ENST00000644933.1:c.*530C>T
|
ENSP00000496133.1:n.*530C>T
|
|
ENST00000645285.1:c.*530C>T
|
ENSP00000495058.1:n.*530C>T
|
|
ENST00000645331.1:n.2869C>T
|
|
|
ENST00000645620.1:c.935C>T
|
ENSP00000493657.1:p.Ala312Val
|
|
ENST00000646691.1:n.1551C>T
|
|
|
ENST00000646777.1:n.1997C>T
|
|
|
ENST00000647016.1:n.2144C>T
|
|
|
ENST00000647152.1:c.935C>T
|
ENSP00000495893.1:p.Ala312Val
|
|
ENST00000647209.1:c.*1533C>T
|
ENSP00000495558.1:n.*1533C>T
|
|
ENST00000647346.1:n.2684C>T
|
|
|
ENST00000299427.10:c.1664C>T
|
ENSP00000299427.6:p.Ala555Val
|
|
ENST00000533371.5:c.935C>T
|
ENSP00000437066.1:p.Ala312Val
|
|
ENST00000611494.4:c.1663C>T
|
ENSP00000484546.1:p.Leu555Phe
|
|
NM_000391.3:c.1664C>T
|
NP_000382.3:p.Ala555Val
|
|
NM_000391.4:c.1664C>T
MANE Select
|
NP_000382.3:p.Ala555Val
|
|