ENST00000352909.8:c.805A>G
MANE Select
|
ENSP00000325951.4:p.Ile269Val
|
|
ENST00000324155.8:c.*494A>G
|
ENSP00000325831.3:n.*494A>G
|
|
ENST00000333684.9:c.696-374A>G
|
ENSP00000328814.6:n.696-374A>G
|
|
ENST00000352909.7:c.805A>G
|
ENSP00000325951.3:p.Ile269Val
|
|
ENST00000381168.7:c.*525A>G
|
ENSP00000370560.3:n.*525A>G
|
|
ENST00000381175.5:c.886A>G
|
ENSP00000370567.1:p.Ile296Val
|
|
ENST00000381178.5:c.898A>G
|
ENSP00000370571.1:p.Ile300Val
|
|
ENST00000412076.1:c.136-374A>G
|
|
|
ENST00000416223.5:c.136-155A>G
|
|
|
ENST00000469226.1:n.934A>G
|
|
|
ENST00000479437.5:n.354A>G
|
|
|
NM_000360.3:c.805A>G
|
NP_000351.2:p.Ile269Val
|
|
NM_199292.2:c.898A>G
|
NP_954986.2:p.Ile300Val
|
|
NM_199293.2:c.886A>G
|
NP_954987.2:p.Ile296Val
|
|
XM_011520335.1:c.817A>G
|
XP_011518637.1:p.Ile273Val
|
|
XM_011520335.2:c.817A>G
|
XP_011518637.1:p.Ile273Val
|
|
NM_000360.4:c.805A>G
MANE Select
|
NP_000351.2:p.Ile269Val
|
|
NM_199292.3:c.898A>G
|
NP_954986.2:p.Ile300Val
|
|
NM_199293.3:c.886A>G
|
NP_954987.2:p.Ile296Val
|
|