ENST00000260210.5:c.1792T>A
MANE Select
|
ENSP00000260210.3:p.Phe598Ile
|
|
ENST00000260210.4:c.1792T>A
|
ENSP00000260210.3:p.Phe598Ile
|
|
ENST00000375445.7:c.1390T>A
|
ENSP00000364594.3:p.Phe464Ile
|
|
ENST00000419189.1:c.567T>A
|
|
|
NM_001159736.1:c.1390T>A
|
NP_001153208.1:p.Phe464Ile
|
|
NM_032725.3:c.1792T>A
|
NP_116114.1:p.Phe598Ile
|
|
XM_011543035.1:c.1693T>A
|
XP_011541337.1:p.Phe565Ile
|
|
XM_011543035.2:c.1693T>A
|
XP_011541337.1:p.Phe565Ile
|
|
NM_032725.4:c.1792T>A
MANE Select
|
NP_116114.1:p.Phe598Ile
|
|
NM_001159736.2:c.1390T>A
|
NP_001153208.1:p.Phe464Ile
|
|