ENST00000324464.8:c.1298C>T
MANE Select
|
ENSP00000315118.3:p.Ala433Val
|
|
ENST00000593724.2:n.3121C>T
|
|
|
ENST00000594490.6:c.1220C>T
|
ENSP00000471310.2:p.Ala407Val
|
|
ENST00000594720.6:c.1298C>T
|
ENSP00000470876.2:p.Ala433Val
|
|
ENST00000596455.6:n.1590C>T
|
|
|
ENST00000601967.6:c.1298C>T
|
ENSP00000470916.2:p.Ala433Val
|
|
ENST00000676555.1:c.*723C>T
|
ENSP00000503387.1:n.*723C>T
|
|
ENST00000676578.1:c.*1040C>T
|
ENSP00000504076.1:n.*1040C>T
|
|
ENST00000676960.1:n.1423C>T
|
|
|
ENST00000676962.1:n.1577C>T
|
|
|
ENST00000677018.1:c.1298C>T
|
ENSP00000503480.1:p.Ala433Val
|
|
ENST00000677039.1:n.3501C>T
|
|
|
ENST00000677399.1:n.1740C>T
|
|
|
ENST00000677496.1:c.971C>T
|
ENSP00000504773.1:p.Ala324Val
|
|
ENST00000677517.1:c.971C>T
|
ENSP00000503519.1:p.Ala324Val
|
|
ENST00000677633.1:c.*721C>T
|
ENSP00000503645.1:n.*721C>T
|
|
ENST00000677800.1:c.*4402C>T
|
ENSP00000503794.1:n.*4402C>T
|
|
ENST00000678057.1:c.*862C>T
|
ENSP00000503762.1:n.*862C>T
|
|
ENST00000678119.1:n.1492C>T
|
|
|
ENST00000678166.1:n.1441C>T
|
|
|
ENST00000678312.1:n.1635C>T
|
|
|
ENST00000678316.1:c.*721C>T
|
ENSP00000504112.1:n.*721C>T
|
|
ENST00000678371.1:n.1748C>T
|
|
|
ENST00000678404.1:c.1298C>T
|
ENSP00000503944.1:p.Ala433Val
|
|
ENST00000678419.1:c.1298C>T
|
ENSP00000504085.1:p.Ala433Val
|
|
ENST00000678433.1:n.1654C>T
|
|
|
ENST00000678467.1:c.1298C>T
|
ENSP00000504072.1:p.Ala433Val
|
|
ENST00000678569.1:c.*283C>T
|
ENSP00000504261.1:n.*283C>T
|
|
ENST00000678961.1:n.1653C>T
|
|
|
ENST00000679002.1:n.1477C>T
|
|
|
ENST00000679012.1:c.854C>T
|
ENSP00000504446.1:p.Ala285Val
|
|
ENST00000679070.1:c.*717C>T
|
ENSP00000503759.1:n.*717C>T
|
|
ENST00000679130.1:c.1298C>T
|
ENSP00000504845.1:p.Ala433Val
|
|
ENST00000679315.1:c.*1128C>T
|
ENSP00000503065.1:n.*1128C>T
|
|
ENST00000243583.10:c.1175C>T
|
ENSP00000243583.5:p.Ala392Val
|
|
ENST00000324464.7:c.1298C>T
|
ENSP00000315118.3:p.Ala433Val
|
|
ENST00000593724.1:n.1413C>T
|
|
|
NM_001142555.2:c.1175C>T
|
NP_001136027.1:p.Ala392Val
|
|
NM_024876.3:c.1298C>T
|
NP_079152.3:p.Ala433Val
|
|
XM_005259270.3:c.1460C>T
|
XP_005259327.2:p.Ala487Val
|
|
XM_005259271.3:c.1298C>T
|
XP_005259328.1:p.Ala433Val
|
|
XM_005259272.3:c.1298C>T
|
XP_005259329.1:p.Ala433Val
|
|
XM_005259273.3:c.1298C>T
|
XP_005259330.1:p.Ala433Val
|
|
XM_006723392.2:c.1298C>T
|
XP_006723455.1:p.Ala433Val
|
|
XM_006723393.2:c.1298C>T
|
XP_006723456.1:p.Ala433Val
|
|
XM_011527334.1:c.1298C>T
|
XP_011525636.1:p.Ala433Val
|
|
XM_011527335.1:c.1157C>T
|
XP_011525637.1:p.Ala386Val
|
|
XM_011527336.1:c.1328C>T
|
XP_011525638.1:p.Ala443Val
|
|
XM_011527337.1:c.1298C>T
|
XP_011525639.1:p.Ala433Val
|
|
XM_011527338.1:c.1298C>T
|
XP_011525640.1:p.Ala433Val
|
|
NM_024876.4:c.1298C>T
MANE Select
|
NP_079152.3:p.Ala433Val
|
|
NM_001142555.3:c.1175C>T
|
NP_001136027.1:p.Ala392Val
|
|