ENST00000352909.8:c.1280A>T
MANE Select
|
ENSP00000325951.4:p.Tyr427Phe
|
|
ENST00000333684.9:c.998A>T
|
ENSP00000328814.6:p.Tyr333Phe
|
|
ENST00000352909.7:c.1280A>T
|
ENSP00000325951.3:p.Tyr427Phe
|
|
ENST00000381175.5:c.1361A>T
|
ENSP00000370567.1:p.Tyr454Phe
|
|
ENST00000381178.5:c.1373A>T
|
ENSP00000370571.1:p.Tyr458Phe
|
|
NM_000360.3:c.1280A>T
|
NP_000351.2:p.Tyr427Phe
|
|
NM_199292.2:c.1373A>T
|
NP_954986.2:p.Tyr458Phe
|
|
NM_199293.2:c.1361A>T
|
NP_954987.2:p.Tyr454Phe
|
|
XM_011520335.1:c.1292A>T
|
XP_011518637.1:p.Tyr431Phe
|
|
XM_011520335.2:c.1292A>T
|
XP_011518637.1:p.Tyr431Phe
|
|
NM_000360.4:c.1280A>T
MANE Select
|
NP_000351.2:p.Tyr427Phe
|
|
NM_199292.3:c.1373A>T
|
NP_954986.2:p.Tyr458Phe
|
|
NM_199293.3:c.1361A>T
|
NP_954987.2:p.Tyr454Phe
|
|