ENST00000352909.8:c.974A>T
MANE Select
|
ENSP00000325951.4:p.Glu325Val
|
|
ENST00000324155.8:c.*663A>T
|
ENSP00000325831.3:n.*663A>T
|
|
ENST00000333684.9:c.696-87A>T
|
ENSP00000328814.6:n.696-87A>T
|
|
ENST00000352909.7:c.974A>T
|
ENSP00000325951.3:p.Glu325Val
|
|
ENST00000381168.7:c.*694A>T
|
ENSP00000370560.3:n.*694A>T
|
|
ENST00000381175.5:c.1055A>T
|
ENSP00000370567.1:p.Glu352Val
|
|
ENST00000381178.5:c.1067A>T
|
ENSP00000370571.1:p.Glu356Val
|
|
ENST00000412076.1:c.136-87A>T
|
|
|
ENST00000416223.5:c.268A>T
|
|
|
ENST00000461172.1:n.139A>T
|
|
|
ENST00000479437.5:n.523A>T
|
|
|
NM_000360.3:c.974A>T
|
NP_000351.2:p.Glu325Val
|
|
NM_199292.2:c.1067A>T
|
NP_954986.2:p.Glu356Val
|
|
NM_199293.2:c.1055A>T
|
NP_954987.2:p.Glu352Val
|
|
XM_011520335.1:c.986A>T
|
XP_011518637.1:p.Glu329Val
|
|
XM_011520335.2:c.986A>T
|
XP_011518637.1:p.Glu329Val
|
|
NM_000360.4:c.974A>T
MANE Select
|
NP_000351.2:p.Glu325Val
|
|
NM_199292.3:c.1067A>T
|
NP_954986.2:p.Glu356Val
|
|
NM_199293.3:c.1055A>T
|
NP_954987.2:p.Glu352Val
|
|