ENST00000344209.10:c.1145A>T
MANE Select
|
ENSP00000345667.5:p.Asp382Val
|
|
ENST00000460554.2:n.1095A>T
|
|
|
ENST00000642615.1:c.*328A>T
|
ENSP00000495499.1:n.*328A>T
|
|
ENST00000273691.7:c.1013A>T
|
ENSP00000273691.3:p.Asp338Val
|
|
ENST00000344209.9:c.1145A>T
|
ENSP00000345667.5:p.Asp382Val
|
|
ENST00000393631.5:c.878A>T
|
ENSP00000377251.1:p.Asp293Val
|
|
ENST00000460554.1:n.1247A>T
|
|
|
ENST00000462014.1:c.1049A>T
|
ENSP00000419414.1:p.Asp350Val
|
|
NM_001199799.1:c.1145A>T
|
NP_001186728.1:p.Asp382Val
|
|
NM_001199800.1:c.878A>T
|
NP_001186729.1:p.Asp293Val
|
|
NM_175924.3:c.1013A>T
|
NP_787120.1:p.Asp338Val
|
|
XM_005247389.3:c.1049A>T
|
XP_005247446.1:p.Asp350Val
|
|
XM_011512738.1:c.1145A>T
|
XP_011511040.1:p.Asp382Val
|
|
XM_011512739.1:c.608A>T
|
XP_011511041.1:p.Asp203Val
|
|
XM_005247389.4:c.1049A>T
|
XP_005247446.1:p.Asp350Val
|
|
XM_011512738.2:c.1145A>T
|
XP_011511040.1:p.Asp382Val
|
|
XM_011512739.2:c.608A>T
|
XP_011511041.1:p.Asp203Val
|
|
NM_001199799.2:c.1145A>T
MANE Select
|
NP_001186728.1:p.Asp382Val
|
|
NM_001199800.2:c.878A>T
|
NP_001186729.1:p.Asp293Val
|
|
NM_175924.4:c.1013A>T
|
NP_787120.1:p.Asp338Val
|
|