ENST00000703544.1:c.*1569G>T
|
ENSP00000515365.1:n.*1569G>T
|
|
ENST00000263253.9:c.3649G>T
MANE Select
|
ENSP00000263253.7:p.Asp1217Tyr
|
|
ENST00000674155.1:c.3571G>T
|
ENSP00000501078.1:p.Asp1191Tyr
|
|
ENST00000263253.8:c.3649G>T
|
ENSP00000263253.7:p.Asp1217Tyr
|
|
NM_001429.3:c.3649G>T
|
NP_001420.2:p.Asp1217Tyr
|
|
XM_006724165.2:c.3571G>T
|
XP_006724228.1:p.Asp1191Tyr
|
|
NM_001362843.1:c.3571G>T
|
NP_001349772.1:p.Asp1191Tyr
|
|
NM_001429.4:c.3649G>T
MANE Select
|
NP_001420.2:p.Asp1217Tyr
|
|
NM_001362843.2:c.3571G>T
|
NP_001349772.1:p.Asp1191Tyr
|
|