ENST00000379727.8:c.*857T>G
MANE Select
|
ENSP00000369050.3:n.*857T>G
|
|
ENST00000379727.7:c.*857T>G
|
ENSP00000369050.3:n.*857T>G
|
|
ENST00000395048.6:c.*857T>G
|
ENSP00000378488.2:n.*857T>G
|
|
ENST00000612821.4:c.2312T>G
|
ENSP00000479744.1:n.2312T>G
|
|
ENST00000617691.4:c.*857T>G
|
ENSP00000482863.1:n.*857T>G
|
|
NM_000499.3:c.*857T>G
|
NP_000490.1:n.*857T>G
|
|
XM_005254185.1:c.*857T>G
|
XP_005254242.1:n.*857T>G
|
|
NM_000499.5:c.*857T>G
|
NP_000490.1:n.*857T>G
|
|
NM_001319216.2:c.*857T>G
|
NP_001306145.1:n.*857T>G
|
|
NM_001319217.2:c.*857T>G
MANE Select
|
NP_001306146.1:n.*857T>G
|
|