|
ENST00000375687.10:c.3962A>T
MANE Select
|
ENSP00000364839.4:p.Asp1321Val
|
|
|
ENST00000646985.1:c.3779A>T
|
ENSP00000495053.1:p.Asp1260Val
|
|
|
ENST00000647223.1:n.6315A>T
|
|
|
|
ENST00000651418.1:c.1870-1756A>T
|
ENSP00000499150.1:n.1870-1756A>T
|
|
|
ENST00000306058.9:c.3947A>T
|
ENSP00000305119.5:p.Asp1316Val
|
|
|
ENST00000375687.8:c.3962A>T
|
ENSP00000364839.4:p.Asp1321Val
|
|
|
ENST00000613218.4:c.3962A>T
|
ENSP00000480487.1:p.Asp1321Val
|
|
|
ENST00000620121.4:c.3962A>T
|
ENSP00000481978.1:p.Asp1321Val
|
|
|
NM_015338.5:c.3962A>T , LRG_630t1:c.3962A>T
|
NP_056153.2:p.Asp1321Val
|
|
|
XM_006723727.2:c.3959A>T
|
XP_006723790.1:p.Asp1320Val
|
|
|
XM_006723728.2:c.3932A>T
|
XP_006723791.1:p.Asp1311Val
|
|
|
XM_006723730.2:c.3878A>T
|
XP_006723793.1:p.Asp1293Val
|
|
|
XM_006723732.2:c.3779A>T
|
XP_006723795.1:p.Asp1260Val
|
|
|
XM_006723733.1:c.3278A>T
|
XP_006723796.1:p.Asp1093Val
|
|
|
XM_011528647.1:c.4226A>T
|
XP_011526949.1:p.Asp1409Val
|
|
|
XM_011528648.1:c.4223A>T
|
XP_011526950.1:p.Asp1408Val
|
|
|
XM_011528649.1:c.4142A>T
|
XP_011526951.1:p.Asp1381Val
|
|
|
XM_011528650.1:c.4073A>T
|
XP_011526952.1:p.Asp1358Val
|
|
|
XM_011528651.1:c.3941A>T
|
XP_011526953.1:p.Asp1314Val
|
|
|
XM_011528652.1:c.3878A>T
|
XP_011526954.1:p.Asp1293Val
|
|
|
NM_001363734.1:c.3779A>T
|
NP_001350663.1:p.Asp1260Val
|
|
|
XM_006723727.3:c.3959A>T
|
XP_006723790.1:p.Asp1320Val
|
|
|
XM_006723728.3:c.3932A>T
|
XP_006723791.1:p.Asp1311Val
|
|
|
XM_006723730.4:c.3878A>T
|
XP_006723793.1:p.Asp1293Val
|
|
|
XM_011528648.3:c.4223A>T
|
XP_011526950.1:p.Asp1408Val
|
|
|
XM_011528652.2:c.3878A>T
|
XP_011526954.1:p.Asp1293Val
|
|
|
XM_017027704.1:c.3878A>T
|
XP_016883193.1:p.Asp1293Val
|
|
|
XM_017027705.1:c.3878A>T
|
XP_016883194.1:p.Asp1293Val
|
|
|
XM_017027706.1:c.3809A>T
|
XP_016883195.1:p.Asp1270Val
|
|
|
NM_015338.6:c.3962A>T
MANE Select
|
NP_056153.2:p.Asp1321Val
|
|
