|
ENST00000265277.10:c.263C>T
|
ENSP00000265277.5:p.Ala88Val
|
|
|
ENST00000451838.2:c.-242-35794C>T
|
ENSP00000408275.2:n.-242-35794C>T
|
|
|
ENST00000480155.2:n.499C>T
|
|
|
|
ENST00000685059.1:c.263C>T
|
ENSP00000510210.1:p.Ala88Val
|
|
|
ENST00000685613.1:c.263C>T
|
ENSP00000510564.1:p.Ala88Val
|
|
|
ENST00000687592.1:n.562C>T
|
|
|
|
ENST00000688928.1:c.263C>T
|
ENSP00000509273.1:p.Ala88Val
|
|
|
ENST00000689118.1:c.263C>T
|
ENSP00000510554.1:p.Ala88Val
|
|
|
ENST00000689300.1:c.263C>T
|
ENSP00000510639.1:p.Ala88Val
|
|
|
ENST00000689997.1:c.-380-21007C>T
|
ENSP00000510700.1:n.-380-21007C>T
|
|
|
ENST00000691151.1:n.555C>T
|
|
|
|
ENST00000691369.1:c.263C>T
|
ENSP00000509754.1:p.Ala88Val
|
|
|
ENST00000691441.1:c.263C>T
|
ENSP00000509686.1:p.Ala88Val
|
|
|
ENST00000691903.1:c.263C>T
|
ENSP00000510314.1:p.Ala88Val
|
|
|
ENST00000692776.1:c.263C>T
|
ENSP00000508524.1:p.Ala88Val
|
|
|
ENST00000369452.9:c.263C>T
MANE Select
|
ENSP00000358464.5:p.Ala88Val
|
|
|
ENST00000265277.9:c.263C>T
|
ENSP00000265277.5:p.Ala88Val
|
|
|
ENST00000369452.8:c.263C>T
|
ENSP00000358464.4:p.Ala88Val
|
|
|
ENST00000489390.1:n.56-35794C>T
|
|
|
|
ENST00000489783.1:n.641C>T
|
|
|
|
NM_001269039.1:c.263C>T
|
NP_001255968.1:p.Ala88Val
|
|
|
NM_007373.3:c.263C>T , LRG_753t1:c.263C>T
|
NP_031399.2:p.Ala88Val
|
|
|
XM_011540216.1:c.-380-21007C>T
|
XP_011538518.1:n.-380-21007C>T
|
|
|
NM_001269039.2:c.263C>T
|
NP_001255968.1:p.Ala88Val
|
|
|
NM_001324336.1:c.263C>T
|
NP_001311265.1:p.Ala88Val
|
|
|
NM_001324337.1:c.263C>T
|
NP_001311266.1:p.Ala88Val
|
|
|
NR_136749.1:n.116-21007C>T
|
|
|
|
NM_007373.4:c.263C>T
MANE Select
|
NP_031399.2:p.Ala88Val
|
|
|
NM_001269039.3:c.263C>T
|
NP_001255968.1:p.Ala88Val
|
|
|
NM_001324336.2:c.263C>T
|
NP_001311265.1:p.Ala88Val
|
|
|
NM_001324337.2:c.263C>T
|
NP_001311266.1:p.Ala88Val
|
|
|
NR_136749.2:n.55-21007C>T
|
|
|
