|
ENST00000703936.1:c.2717A>T
|
ENSP00000515567.1:p.Asp906Val
|
|
|
ENST00000703937.1:c.*1778A>T
|
ENSP00000515568.1:n.*1778A>T
|
|
|
ENST00000326739.9:c.677A>T
MANE Select
|
ENSP00000321584.4:p.Asp226Val
|
|
|
ENST00000429182.6:c.677A>T
|
ENSP00000393525.2:p.Asp226Val
|
|
|
ENST00000442157.2:c.602A>T
|
ENSP00000403502.2:p.Asp201Val
|
|
|
ENST00000462980.2:n.1192A>T
|
|
|
|
ENST00000472328.2:n.743A>T
|
|
|
|
ENST00000491610.2:n.637A>T
|
|
|
|
ENST00000676607.1:n.973A>T
|
|
|
|
ENST00000676627.1:n.1407A>T
|
|
|
|
ENST00000676708.1:n.1957A>T
|
|
|
|
ENST00000676864.1:n.1826A>T
|
|
|
|
ENST00000677010.1:c.713A>T
|
ENSP00000503089.1:p.Asp238Val
|
|
|
ENST00000677108.1:n.2583A>T
|
|
|
|
ENST00000677168.1:n.1149A>T
|
|
|
|
ENST00000677185.1:n.1240A>T
|
|
|
|
ENST00000677205.1:n.1461A>T
|
|
|
|
ENST00000677344.1:n.1951A>T
|
|
|
|
ENST00000677480.1:c.*354A>T
|
ENSP00000504378.1:n.*354A>T
|
|
|
ENST00000677519.1:n.1387A>T
|
|
|
|
ENST00000677593.1:n.1233A>T
|
|
|
|
ENST00000677740.1:n.2182A>T
|
|
|
|
ENST00000677991.1:n.1850A>T
|
|
|
|
ENST00000678001.1:n.1170A>T
|
|
|
|
ENST00000678085.1:n.1233A>T
|
|
|
|
ENST00000678177.1:n.2526A>T
|
|
|
|
ENST00000678603.1:n.1755A>T
|
|
|
|
ENST00000678724.1:c.602A>T
|
ENSP00000503874.1:p.Asp201Val
|
|
|
ENST00000678920.1:n.835A>T
|
|
|
|
ENST00000679019.1:n.1447A>T
|
|
|
|
ENST00000679117.1:c.*492A>T
|
ENSP00000503240.1:n.*492A>T
|
|
|
ENST00000679339.1:n.1518A>T
|
|
|
|
ENST00000326739.8:c.677A>T
|
ENSP00000321584.4:p.Asp226Val
|
|
|
ENST00000429182.5:c.471A>T
|
|
|
|
ENST00000442157.1:c.602A>T
|
ENSP00000403502.1:p.Asp201Val
|
|
|
ENST00000462980.1:n.579A>T
|
|
|
|
ENST00000491610.1:n.637A>T
|
|
|
|
NM_000884.2:c.677A>T
|
NP_000875.2:p.Asp226Val
|
|
|
XM_006713128.2:c.887A>T
|
XP_006713191.1:p.Asp296Val
|
|
|
XM_006713128.3:c.887A>T
|
XP_006713191.1:p.Asp296Val
|
|
|
XM_017006349.1:c.812A>T
|
XP_016861838.1:p.Asp271Val
|
|
|
XM_017006350.1:c.812A>T
|
XP_016861839.1:p.Asp271Val
|
|
|
NM_000884.3:c.677A>T
MANE Select
|
NP_000875.2:p.Asp226Val
|
|
