ENST00000352909.8:c.642G=
MANE Select
|
ENSP00000325951.4:p.Arg214=
|
|
ENST00000324155.8:c.*331G=
|
ENSP00000325831.3:n.*331G=
|
|
ENST00000333684.9:c.642G=
|
ENSP00000328814.6:p.Arg214=
|
|
ENST00000352909.7:c.642G=
|
ENSP00000325951.3:p.Arg214=
|
|
ENST00000381168.7:c.*331G=
|
ENSP00000370560.3:n.*331G=
|
|
ENST00000381175.5:c.723G=
|
ENSP00000370567.1:p.Arg241=
|
|
ENST00000381178.5:c.735G=
|
ENSP00000370571.1:p.Arg245=
|
|
ENST00000412076.1:c.82G=
|
|
|
ENST00000416223.5:c.82G=
|
|
|
ENST00000469226.1:n.391G=
|
|
|
NM_000360.3:c.642G=
|
NP_000351.2:p.Arg214=
|
|
NM_199292.2:c.735G=
|
NP_954986.2:p.Arg245=
|
|
NM_199293.2:c.723G=
|
NP_954987.2:p.Arg241=
|
|
XM_011520335.1:c.654G=
|
XP_011518637.1:p.Arg218=
|
|
XM_011520335.2:c.654G=
|
XP_011518637.1:p.Arg218=
|
|
NM_000360.4:c.642G=
MANE Select
|
NP_000351.2:p.Arg214=
|
|
NM_199292.3:c.735G=
|
NP_954986.2:p.Arg245=
|
|
NM_199293.3:c.723G=
|
NP_954987.2:p.Arg241=
|
|