ENST00000352909.8:c.806T>A
MANE Select
|
ENSP00000325951.4:p.Ile269Asn
|
|
ENST00000324155.8:c.*495T>A
|
ENSP00000325831.3:n.*495T>A
|
|
ENST00000333684.9:c.696-373T>A
|
ENSP00000328814.6:n.696-373T>A
|
|
ENST00000352909.7:c.806T>A
|
ENSP00000325951.3:p.Ile269Asn
|
|
ENST00000381168.7:c.*526T>A
|
ENSP00000370560.3:n.*526T>A
|
|
ENST00000381175.5:c.887T>A
|
ENSP00000370567.1:p.Ile296Asn
|
|
ENST00000381178.5:c.899T>A
|
ENSP00000370571.1:p.Ile300Asn
|
|
ENST00000412076.1:c.136-373T>A
|
|
|
ENST00000416223.5:c.136-154T>A
|
|
|
ENST00000469226.1:n.935T>A
|
|
|
ENST00000479437.5:n.355T>A
|
|
|
NM_000360.3:c.806T>A
|
NP_000351.2:p.Ile269Asn
|
|
NM_199292.2:c.899T>A
|
NP_954986.2:p.Ile300Asn
|
|
NM_199293.2:c.887T>A
|
NP_954987.2:p.Ile296Asn
|
|
XM_011520335.1:c.818T>A
|
XP_011518637.1:p.Ile273Asn
|
|
XM_011520335.2:c.818T>A
|
XP_011518637.1:p.Ile273Asn
|
|
NM_000360.4:c.806T>A
MANE Select
|
NP_000351.2:p.Ile269Asn
|
|
NM_199292.3:c.899T>A
|
NP_954986.2:p.Ile300Asn
|
|
NM_199293.3:c.887T>A
|
NP_954987.2:p.Ile296Asn
|
|