ENST00000352909.8:c.1486A>T
MANE Select
|
ENSP00000325951.4:p.Ile496Phe
|
|
ENST00000333684.9:c.1204A>T
|
ENSP00000328814.6:p.Ile402Phe
|
|
ENST00000352909.7:c.1486A>T
|
ENSP00000325951.3:p.Ile496Phe
|
|
ENST00000381175.5:c.1567A>T
|
ENSP00000370567.1:p.Ile523Phe
|
|
ENST00000381178.5:c.1579A>T
|
ENSP00000370571.1:p.Ile527Phe
|
|
NM_000360.3:c.1486A>T
|
NP_000351.2:p.Ile496Phe
|
|
NM_199292.2:c.1579A>T
|
NP_954986.2:p.Ile527Phe
|
|
NM_199293.2:c.1567A>T
|
NP_954987.2:p.Ile523Phe
|
|
XM_011520335.1:c.1498A>T
|
XP_011518637.1:p.Ile500Phe
|
|
XM_011520335.2:c.1498A>T
|
XP_011518637.1:p.Ile500Phe
|
|
NM_000360.4:c.1486A>T
MANE Select
|
NP_000351.2:p.Ile496Phe
|
|
NM_199292.3:c.1579A>T
|
NP_954986.2:p.Ile527Phe
|
|
NM_199293.3:c.1567A>T
|
NP_954987.2:p.Ile523Phe
|
|