|
ENST00000361492.9:c.1346A>T
MANE Select
|
ENSP00000354586.5:p.Glu449Val
|
|
|
ENST00000452319.6:c.1397A>T
|
ENSP00000390436.1:p.Glu466Val
|
|
|
ENST00000314490.15:c.410A>T
|
ENSP00000312694.12:p.Glu137Val
|
|
|
ENST00000341310.10:c.*445A>T
|
ENSP00000344473.6:n.*445A>T
|
|
|
ENST00000361492.8:c.1397A>T
|
ENSP00000354586.4:p.Glu466Val
|
|
|
ENST00000435313.6:n.1371A>T
|
|
|
|
ENST00000437950.5:c.*496A>T
|
ENSP00000415773.1:n.*496A>T
|
|
|
ENST00000438299.5:c.*496A>T
|
ENSP00000400593.1:n.*496A>T
|
|
|
ENST00000445186.5:c.*496A>T
|
ENSP00000397488.1:n.*496A>T
|
|
|
ENST00000452319.5:c.1397A>T
|
ENSP00000390436.1:p.Glu466Val
|
|
|
ENST00000452692.5:c.*445A>T
|
ENSP00000403715.1:n.*445A>T
|
|
|
NM_005270.4:c.1397A>T
|
NP_005261.2:p.Glu466Val
|
|
|
XM_006712422.1:c.1346A>T
|
XP_006712485.1:p.Glu449Val
|
|
|
XM_011510969.1:c.1379A>T
|
XP_011509271.1:p.Glu460Val
|
|
|
XM_011510970.1:c.1256A>T
|
XP_011509272.1:p.Glu419Val
|
|
|
XM_011510971.1:c.1202A>T
|
XP_011509273.1:p.Glu401Val
|
|
|
XM_011510972.1:c.1202A>T
|
XP_011509274.1:p.Glu401Val
|
|
|
XM_011510973.1:c.1022A>T
|
XP_011509275.1:p.Glu341Val
|
|
|
XM_011510974.1:c.971A>T
|
XP_011509276.1:p.Glu324Val
|
|
|
XM_006712422.3:c.1346A>T
|
XP_006712485.1:p.Glu449Val
|
|
|
XM_011510969.2:c.1649A>T
|
XP_011509271.2:p.Glu550Val
|
|
|
XM_011510970.2:c.1256A>T
|
XP_011509272.1:p.Glu419Val
|
|
|
XM_011510971.2:c.1202A>T
|
XP_011509273.1:p.Glu401Val
|
|
|
XM_011510972.2:c.1298A>T
|
XP_011509274.2:p.Glu433Val
|
|
|
XM_011510973.2:c.1022A>T
|
XP_011509275.1:p.Glu341Val
|
|
|
XM_011510974.2:c.971A>T
|
XP_011509276.1:p.Glu324Val
|
|
|
XM_017003818.1:c.1598A>T
|
XP_016859307.1:p.Glu533Val
|
|
|
XM_024452794.1:c.1397A>T
|
XP_024308562.1:p.Glu466Val
|
|
|
XM_024452795.1:c.1397A>T
|
XP_024308563.1:p.Glu466Val
|
|
|
NM_001371271.1:c.1397A>T
|
NP_001358200.1:p.Glu466Val
|
|
|
NM_001374353.1:c.1346A>T
MANE Select
|
NP_001361282.1:p.Glu449Val
|
|
|
NM_001374354.1:c.971A>T
|
NP_001361283.1:p.Glu324Val
|
|
|
NM_005270.5:c.1397A>T
|
NP_005261.2:p.Glu466Val
|
|
