ENST00000396954.8:c.529A>T
MANE Select
|
ENSP00000380157.3:p.Lys177Ter
|
|
ENST00000450852.8:c.*449A>T
MANE Plus Clinical
|
ENSP00000411022.3:n.*449A>T
|
|
ENST00000361377.8:c.*298A>T
|
ENSP00000355160.4:n.*298A>T
|
|
ENST00000396954.7:c.529A>T
|
ENSP00000380157.3:p.Lys177Ter
|
|
ENST00000450852.7:c.*449A>T
|
ENSP00000411022.3:n.*449A>T
|
|
ENST00000502402.5:n.2276A>T
|
|
|
ENST00000508922.5:c.*369A>T
|
ENSP00000426274.1:n.*369A>T
|
|
ENST00000510818.6:c.*402A>T
|
ENSP00000424267.2:n.*402A>T
|
|
ENST00000582677.5:c.*170A>T
|
ENSP00000462870.1:n.*170A>T
|
|
ENST00000584946.5:c.*321A>T
|
ENSP00000464663.1:n.*321A>T
|
|
NM_004531.4:c.529A>T
|
NP_004522.1:p.Lys177Ter
|
|
NM_176806.3:c.*449A>T
|
NP_789776.1:n.*449A>T
|
|
NM_004531.5:c.529A>T
MANE Select
|
NP_004522.1:p.Lys177Ter
|
|
NM_176806.4:c.*449A>T
MANE Plus Clinical
|
NP_789776.1:n.*449A>T
|
|