ENST00000352909.8:c.772C>G
MANE Select
|
ENSP00000325951.4:p.Leu258Val
|
|
ENST00000324155.8:c.*461C>G
|
ENSP00000325831.3:n.*461C>G
|
|
ENST00000333684.9:c.696-407C>G
|
ENSP00000328814.6:n.696-407C>G
|
|
ENST00000352909.7:c.772C>G
|
ENSP00000325951.3:p.Leu258Val
|
|
ENST00000381168.7:c.*492C>G
|
ENSP00000370560.3:n.*492C>G
|
|
ENST00000381175.5:c.853C>G
|
ENSP00000370567.1:p.Leu285Val
|
|
ENST00000381178.5:c.865C>G
|
ENSP00000370571.1:p.Leu289Val
|
|
ENST00000412076.1:c.136-407C>G
|
|
|
ENST00000416223.5:c.136-188C>G
|
|
|
ENST00000469226.1:n.901C>G
|
|
|
ENST00000479437.5:n.321C>G
|
|
|
NM_000360.3:c.772C>G
|
NP_000351.2:p.Leu258Val
|
|
NM_199292.2:c.865C>G
|
NP_954986.2:p.Leu289Val
|
|
NM_199293.2:c.853C>G
|
NP_954987.2:p.Leu285Val
|
|
XM_011520335.1:c.784C>G
|
XP_011518637.1:p.Leu262Val
|
|
XM_011520335.2:c.784C>G
|
XP_011518637.1:p.Leu262Val
|
|
NM_000360.4:c.772C>G
MANE Select
|
NP_000351.2:p.Leu258Val
|
|
NM_199292.3:c.865C>G
|
NP_954986.2:p.Leu289Val
|
|
NM_199293.3:c.853C>G
|
NP_954987.2:p.Leu285Val
|
|