ENST00000295497.13:c.*657G>A
|
ENSP00000295497.7:n.*657G>A
|
|
ENST00000295497.12:c.*657G>A
|
ENSP00000295497.7:n.*657G>A
|
|
ENST00000409900.9:c.*657G>A
MANE Select
|
ENSP00000386741.4:n.*657G>A
|
|
ENST00000443238.6:c.*657G>A
|
ENSP00000409798.2:n.*657G>A
|
|
ENST00000652036.1:c.*657G>A
|
ENSP00000499139.1:n.*657G>A
|
|
ENST00000409900.7:c.*657G>A
|
ENSP00000386741.3:n.*657G>A
|
|
NM_001025201.3:c.*657G>A
|
NP_001020372.2:n.*657G>A
|
|
NM_001206602.1:c.*657G>A
|
NP_001193531.1:n.*657G>A
|
|
NM_001822.5:c.*657G>A
|
NP_001813.1:n.*657G>A
|
|
NR_038133.1:n.1903G>A
|
|
|
NM_001025201.4:c.*657G>A
|
NP_001020372.2:n.*657G>A
|
|
NM_001206602.2:c.*657G>A
|
NP_001193531.1:n.*657G>A
|
|
NM_001371513.1:c.*657G>A
|
NP_001358442.1:n.*657G>A
|
|
NM_001371514.1:c.*657G>A
|
NP_001358443.1:n.*657G>A
|
|
NM_001822.7:c.*657G>A
MANE Select
|
NP_001813.1:n.*657G>A
|
|
NR_038133.2:n.1905G>A
|
|
|