ENST00000494417.2:n.853C>T
|
|
|
ENST00000683044.1:c.749C>T
|
ENSP00000507095.1:p.Ala250Val
|
|
ENST00000683288.1:c.*748C>T
|
ENSP00000507477.1:n.*748C>T
|
|
ENST00000683331.1:n.696C>T
|
|
|
ENST00000683748.1:c.749C>T
|
ENSP00000507377.1:p.Ala250Val
|
|
ENST00000683905.1:c.749C>T
|
ENSP00000506960.1:p.Ala250Val
|
|
ENST00000684139.1:c.433-1494C>T
|
ENSP00000507295.1:n.433-1494C>T
|
|
ENST00000684210.1:n.467C>T
|
|
|
ENST00000684314.1:c.749C>T
|
ENSP00000507700.1:p.Ala250Val
|
|
ENST00000684331.1:c.749C>T
|
ENSP00000507431.1:p.Ala250Val
|
|
ENST00000684646.1:c.749C>T
|
ENSP00000507723.1:p.Ala250Val
|
|
ENST00000309971.9:c.749C>T
MANE Select
|
ENSP00000308622.5:p.Ala250Val
|
|
ENST00000309971.8:c.749C>T
|
ENSP00000308622.4:p.Ala250Val
|
|
ENST00000372770.4:c.749C>T
|
ENSP00000361856.4:p.Ala250Val
|
|
ENST00000494417.1:n.51C>T
|
|
|
NM_001003722.1:c.749C>T , LRG_484t1:c.749C>T
|
NP_001003722.1:p.Ala250Val
|
|
NM_001499.2:c.749C>T , LRG_484t2:c.749C>T
|
NP_001490.1:p.Ala250Val
|
|
XM_006717059.2:c.758C>T
|
XP_006717122.1:p.Ala253Val
|
|
XM_006717060.2:c.758C>T
|
XP_006717123.1:p.Ala253Val
|
|
XM_011518549.1:c.758C>T
|
XP_011516851.1:p.Ala253Val
|
|
XM_011518550.1:c.758C>T
|
XP_011516852.1:p.Ala253Val
|
|
XM_011518551.1:c.749C>T
|
XP_011516853.1:p.Ala250Val
|
|
XM_011518552.1:c.4C>T
|
XP_011516854.1:p.Leu2Phe
|
|
XM_006717059.3:c.758C>T
|
XP_006717122.1:p.Ala253Val
|
|
XM_006717060.3:c.758C>T
|
XP_006717123.1:p.Ala253Val
|
|
XM_011518551.2:c.749C>T
|
XP_011516853.1:p.Ala250Val
|
|
XM_024447519.1:c.758C>T
|
XP_024303287.1:p.Ala253Val
|
|
NM_001003722.2:c.749C>T
MANE Select
|
NP_001003722.1:p.Ala250Val
|
|