|
ENST00000303391.11:c.836C>T
MANE Plus Clinical
|
ENSP00000301948.6:p.Ala279Val
|
|
|
ENST00000453960.7:c.872C>T
MANE Select
|
ENSP00000395535.2:p.Ala291Val
|
|
|
ENST00000637917.1:c.66-56C>T
|
|
|
|
ENST00000303391.10:c.836C>T
|
ENSP00000301948.6:p.Ala279Val
|
|
|
ENST00000407218.5:c.*208C>T
|
ENSP00000384865.2:n.*208C>T
|
|
|
ENST00000453960.6:c.872C>T
|
ENSP00000395535.2:p.Ala291Val
|
|
|
ENST00000619732.4:c.836C>T
|
ENSP00000480973.1:p.Ala279Val
|
|
|
ENST00000622433.4:c.824C>T
|
ENSP00000484470.1:p.Ala275Val
|
|
|
ENST00000628176.2:c.*208C>T
|
ENSP00000486978.1:n.*208C>T
|
|
|
NM_001110792.1:c.872C>T
|
NP_001104262.1:p.Ala291Val
|
|
|
NM_001316337.1:c.557C>T
|
NP_001303266.1:p.Ala186Val
|
|
|
NM_004992.3:c.836C>T
|
NP_004983.1:p.Ala279Val
|
|
|
XM_005274681.3:c.836C>T
|
XP_005274738.1:p.Ala279Val
|
|
|
XM_005274682.3:c.557C>T
|
XP_005274739.1:p.Ala186Val
|
|
|
XM_005274683.3:c.557C>T
|
XP_005274740.1:p.Ala186Val
|
|
|
XM_006724819.2:c.167C>T
|
XP_006724882.1:p.Ala56Val
|
|
|
XM_011531166.1:c.557C>T
|
XP_011529468.1:p.Ala186Val
|
|
|
XM_006724819.3:c.167C>T
|
XP_006724882.1:p.Ala56Val
|
|
|
XM_011531166.2:c.557C>T
|
XP_011529468.1:p.Ala186Val
|
|
|
XM_024452383.1:c.557C>T
|
XP_024308151.1:p.Ala186Val
|
|
|
XM_024452384.1:c.557C>T
|
XP_024308152.1:p.Ala186Val
|
|
|
NM_001110792.2:c.872C>T
MANE Select
|
NP_001104262.1:p.Ala291Val
|
|
|
NM_001316337.2:c.557C>T
|
NP_001303266.1:p.Ala186Val
|
|
|
NM_001369391.2:c.557C>T
|
NP_001356320.1:p.Ala186Val
|
|
|
NM_001369392.2:c.557C>T
|
NP_001356321.1:p.Ala186Val
|
|
|
NM_001369393.2:c.557C>T
|
NP_001356322.1:p.Ala186Val
|
|
|
NM_001369394.1:c.557C>T
|
NP_001356323.1:p.Ala186Val
|
|
|
NM_001369394.2:c.557C>T
|
NP_001356323.1:p.Ala186Val
|
|
|
NM_001386137.1:c.167C>T
|
NP_001373066.1:p.Ala56Val
|
|
|
NM_001386138.1:c.167C>T
|
NP_001373067.1:p.Ala56Val
|
|
|
NM_001386139.1:c.167C>T
|
NP_001373068.1:p.Ala56Val
|
|
|
NM_004992.4:c.836C>T
MANE Plus Clinical
|
NP_004983.1:p.Ala279Val
|
|
