ENST00000613132.5:c.*77G>T
MANE Select
|
ENSP00000477772.2:n.*77G>T
|
|
ENST00000381083.9:c.*77G>T
|
ENSP00000370473.4:n.*77G>T
|
|
ENST00000275521.10:c.*77G>T
|
ENSP00000275521.5:n.*77G>T
|
|
ENST00000381086.9:c.*77G>T
|
ENSP00000370476.4:n.*77G>T
|
|
ENST00000460209.1:n.583G>T
|
|
|
ENST00000613132.4:c.890G>T
|
ENSP00000477772.1:n.890G>T
|
|
NM_000598.4:c.*77G>T
|
NP_000589.2:n.*77G>T
|
|
NM_001013398.1:c.*77G>T
|
NP_001013416.1:n.*77G>T
|
|
NM_001013398.2:c.*77G>T
|
NP_001013416.1:n.*77G>T
|
|
NM_000598.5:c.*77G>T
MANE Select
|
NP_000589.2:n.*77G>T
|
|