ENST00000357578.8:c.531C>T
MANE Select
|
ENSP00000350191.3:p.Asp177=
|
|
ENST00000672352.1:c.294C>T
|
ENSP00000500876.1:p.Asp98=
|
|
ENST00000672557.1:c.449C>T
|
|
|
ENST00000672652.1:c.452C>T
|
|
|
ENST00000675422.1:n.1291C>T
|
|
|
ENST00000348925.2:c.531C>T
|
ENSP00000314649.3:p.Asp177=
|
|
ENST00000357578.7:c.531C>T
|
ENSP00000350191.3:p.Asp177=
|
|
ENST00000491546.5:c.447C>T
|
ENSP00000417687.1:p.Asp149=
|
|
NM_001080.3:c.531C>T
MANE Select
|
NP_001071.1:p.Asp177=
|
|
NM_170740.1:c.531C>T
|
NP_733936.1:p.Asp177=
|
|
NM_001368954.1:c.531C>T
|
NP_001355883.1:p.Asp177=
|
|