ENST00000480266.6:c.*485G>T
|
ENSP00000479015.1:n.*485G>T
|
|
ENST00000373203.9:c.*485G>T
MANE Select
|
ENSP00000362299.4:n.*485G>T
|
|
ENST00000344849.4:c.*720G>T
|
ENSP00000341917.3:n.*720G>T
|
|
ENST00000373203.8:c.*485G>T
|
ENSP00000362299.4:n.*485G>T
|
|
ENST00000480266.5:c.*485G>T
|
ENSP00000479015.1:n.*485G>T
|
|
NM_000118.3:c.*720G>T , LRG_589t1:c.*720G>T
|
NP_000109.1:n.*720G>T
|
|
NM_001114753.2:c.*485G>T , LRG_589t2:c.*485G>T
|
NP_001108225.1:n.*485G>T
|
|
NM_001278138.1:c.*485G>T
|
NP_001265067.1:n.*485G>T
|
|
NM_001114753.3:c.*485G>T
MANE Select
|
NP_001108225.1:n.*485G>T
|
|
NM_001278138.2:c.*485G>T
|
NP_001265067.1:n.*485G>T
|
|