ENST00000329198.5:c.411G>C
MANE Select
|
ENSP00000327758.4:p.Arg137=
|
|
ENST00000329198.4:c.411G>C
|
ENSP00000327758.4:p.Arg137=
|
|
ENST00000424406.2:c.*364G>C
|
ENSP00000395378.2:n.*364G>C
|
|
ENST00000521848.1:c.*210G>C
|
ENSP00000427906.1:n.*210G>C
|
|
NM_001166175.1:c.*364G>C
|
NP_001159647.1:n.*364G>C
|
|
NM_001166176.1:c.*210G>C
|
NP_001159648.1:n.*210G>C
|
|
NM_004387.3:c.411G>C
|
NP_004378.1:p.Arg137=
|
|
NM_004387.4:c.411G>C
MANE Select
|
NP_004378.1:p.Arg137=
|
|
NM_001166175.2:c.*364G>C
|
NP_001159647.1:n.*364G>C
|
|
NM_001166176.2:c.*210G>C
|
NP_001159648.1:n.*210G>C
|
|