|
NM_182925.5:c.3821A>T
MANE Select
|
NP_891555.2:p.Asp1274Val
|
|
ENST00000261937.11:c.3821A>T
MANE Select
|
ENSP00000261937.6:p.Asp1274Val
|
|
NM_001354989.1:c.3821A>T
|
NP_001341918.1:p.Asp1274Val
|
|
NM_001354989.2:c.3821A>T
|
NP_001341918.1:p.Asp1274Val
|
|
NM_002020.4:c.3821A>T
|
NP_002011.2:p.Asp1274Val
|
|
NM_002020.5:c.3821A>T
|
NP_002011.2:p.Asp1274Val
|
|
NM_182925.4:c.3821A>T
|
NP_891555.2:p.Asp1274Val
|
|
ENST00000261937.10:c.3821A>T
|
ENSP00000261937.6:p.Asp1274Val
|
|
ENST00000393347.7:c.3821A>T
|
ENSP00000377016.3:p.Asp1274Val
|
|
ENST00000502603.5:n.521A>T
|
|
|
ENST00000502649.5:c.3821A>T
|
ENSP00000426057.1:p.Asp1274Val
|
|
ENST00000507059.5:n.5022A>T
|
|
|
ENST00000619105.4:c.*2764A>T
|
ENSP00000481134.1:n.*2764A>T
|
|
XM_011534477.1:c.4070A>T
|
XP_011532779.1:p.Asp1357Val
|
|
XM_011534478.1:c.4052A>T
|
XP_011532780.1:p.Asp1351Val
|
|
XM_011534478.3:c.4052A>T
|
XP_011532780.1:p.Asp1351Val
|
|
XM_011534479.1:c.4143A>T
|
XP_011532781.1:p.Arg1381Ser
|
|
XM_011534480.1:c.4143A>T
|
XP_011532782.1:p.Arg1381Ser
|
|
XM_011534481.1:c.4070A>T
|
XP_011532783.1:p.Asp1357Val
|
|
XM_011534482.1:c.3839A>T
|
XP_011532784.1:p.Asp1280Val
|
|
XM_011534483.1:c.3761A>T
|
XP_011532785.1:p.Asp1254Val
|
|
XM_011534484.1:c.3362A>T
|
XP_011532786.1:p.Asp1121Val
|
|
XM_011534484.2:c.3362A>T
|
XP_011532786.1:p.Asp1121Val
|
|
XM_017009263.1:c.4125A>T
|
XP_016864752.1:p.Arg1375Ser
|
|
XM_017009264.2:c.4125A>T
|
XP_016864753.1:p.Arg1375Ser
|
|
XM_017009265.1:c.4125A>T
|
XP_016864754.1:p.Arg1375Ser
|
|
XM_017009266.1:c.4052A>T
|
XP_016864755.1:p.Asp1351Val
|
|
XM_017009267.2:c.4052A>T
|
XP_016864756.1:p.Asp1351Val
|
|
XM_017009268.1:c.3743A>T
|
XP_016864757.1:p.Asp1248Val
|
|
XR_001742050.2:n.4311A>T
|
|
|
XR_941095.1:n.4107A>T
|
|
