|
ENST00000378156.9:c.4100A>T
MANE Select
|
ENSP00000367398.4:p.Asp1367Val
|
|
|
ENST00000378156.8:c.4100A>T
|
ENSP00000367398.4:p.Asp1367Val
|
|
|
ENST00000378161.5:n.3251A>T
|
|
|
|
ENST00000378169.7:c.*3001A>T
|
ENSP00000367411.3:n.*3001A>T
|
|
|
ENST00000460696.1:n.2848A>T
|
|
|
|
ENST00000478423.6:n.3832A>T
|
|
|
|
ENST00000489180.6:c.*1911A>T
|
ENSP00000423747.1:n.*1911A>T
|
|
|
NM_001291593.1:c.2561A>T
|
NP_001278522.1:p.Asp854Val
|
|
|
NM_001291594.1:c.2564A>T
|
NP_001278523.1:p.Asp855Val
|
|
|
NM_015102.4:c.4100A>T
|
NP_055917.1:p.Asp1367Val
|
|
|
NR_111987.1:n.4915A>T
|
|
|
|
XM_006710563.2:c.4100A>T
|
XP_006710626.1:p.Asp1367Val
|
|
|
XM_006710565.2:c.4100A>T
|
XP_006710628.1:p.Asp1367Val
|
|
|
XM_011541213.1:c.4097A>T
|
XP_011539515.1:p.Asp1366Val
|
|
|
XM_011541214.1:c.4058A>T
|
XP_011539516.1:p.Asp1353Val
|
|
|
XM_011541215.1:c.3989A>T
|
XP_011539517.1:p.Asp1330Val
|
|
|
XM_011541216.1:c.4100A>T
|
XP_011539518.1:p.Asp1367Val
|
|
|
XM_011541217.1:c.4100A>T
|
XP_011539519.1:p.Asp1367Val
|
|
|
XM_011541218.1:c.4100A>T
|
XP_011539520.1:p.Asp1367Val
|
|
|
XM_011541219.1:c.4046A>T
|
XP_011539521.1:p.Asp1349Val
|
|
|
XM_006710563.3:c.4100A>T
|
XP_006710626.1:p.Asp1367Val
|
|
|
XM_011541216.2:c.4100A>T
|
XP_011539518.1:p.Asp1367Val
|
|
|
XM_011541217.2:c.4100A>T
|
XP_011539519.1:p.Asp1367Val
|
|
|
XM_011541218.2:c.4100A>T
|
XP_011539520.1:p.Asp1367Val
|
|
|
XM_017000996.1:c.4055A>T
|
XP_016856485.1:p.Asp1352Val
|
|
|
XM_017000997.1:c.4100A>T
|
XP_016856486.1:p.Asp1367Val
|
|
|
XM_017000999.1:c.3572A>T
|
XP_016856488.1:p.Asp1191Val
|
|
|
XM_017001000.2:c.3572A>T
|
XP_016856489.1:p.Asp1191Val
|
|
|
XM_017001001.1:c.3302A>T
|
XP_016856490.1:p.Asp1101Val
|
|
|
XM_017001003.1:c.2561A>T
|
XP_016856492.1:p.Asp854Val
|
|
|
XR_001737114.1:n.3966A>T
|
|
|
|
XR_001737115.1:n.3951A>T
|
|
|
|
NM_015102.5:c.4100A>T
MANE Select
|
NP_055917.1:p.Asp1367Val
|
|
|
NM_001291593.2:c.2561A>T
|
NP_001278522.1:p.Asp854Val
|
|
|
NM_001291594.2:c.2564A>T
|
NP_001278523.1:p.Asp855Val
|
|
|
NR_111987.2:n.4867A>T
|
|
|
