ENST00000621467.5:c.*3046C>T
|
ENSP00000480508.2:n.*3046C>T
|
|
ENST00000686475.1:n.4213C>T
|
|
|
ENST00000409883.7:c.*3046C>T
MANE Select
|
ENSP00000386264.2:n.*3046C>T
|
|
ENST00000409444.6:c.*3046C>T
|
ENSP00000387203.2:n.*3046C>T
|
|
ENST00000409883.6:c.*3046C>T
|
ENSP00000386264.2:n.*3046C>T
|
|
ENST00000495329.1:n.3412C>T
|
|
|
NM_001044385.2:c.*3046C>T
|
NP_001037850.1:n.*3046C>T
|
|
NM_152388.3:c.*3046C>T
|
NP_689601.2:n.*3046C>T
|
|
NM_001044385.3:c.*3046C>T
MANE Select
|
NP_001037850.1:n.*3046C>T
|
|
NM_152388.4:c.*3046C>T
|
NP_689601.2:n.*3046C>T
|
|