ENST00000352909.8:c.640A>G
MANE Select
|
ENSP00000325951.4:p.Arg214Gly
|
|
ENST00000324155.8:c.*329A>G
|
ENSP00000325831.3:n.*329A>G
|
|
ENST00000333684.9:c.640A>G
|
ENSP00000328814.6:p.Arg214Gly
|
|
ENST00000352909.7:c.640A>G
|
ENSP00000325951.3:p.Arg214Gly
|
|
ENST00000381168.7:c.*329A>G
|
ENSP00000370560.3:n.*329A>G
|
|
ENST00000381175.5:c.721A>G
|
ENSP00000370567.1:p.Arg241Gly
|
|
ENST00000381178.5:c.733A>G
|
ENSP00000370571.1:p.Arg245Gly
|
|
ENST00000412076.1:c.80A>G
|
|
|
ENST00000416223.5:c.80A>G
|
|
|
ENST00000469226.1:n.389A>G
|
|
|
NM_000360.3:c.640A>G
|
NP_000351.2:p.Arg214Gly
|
|
NM_199292.2:c.733A>G
|
NP_954986.2:p.Arg245Gly
|
|
NM_199293.2:c.721A>G
|
NP_954987.2:p.Arg241Gly
|
|
XM_011520335.1:c.652A>G
|
XP_011518637.1:p.Arg218Gly
|
|
XM_011520335.2:c.652A>G
|
XP_011518637.1:p.Arg218Gly
|
|
NM_000360.4:c.640A>G
MANE Select
|
NP_000351.2:p.Arg214Gly
|
|
NM_199292.3:c.733A>G
|
NP_954986.2:p.Arg245Gly
|
|
NM_199293.3:c.721A>G
|
NP_954987.2:p.Arg241Gly
|
|