ENST00000352909.8:c.721G>C
MANE Select
|
ENSP00000325951.4:p.Gly241Arg
|
|
ENST00000324155.8:c.*410G>C
|
ENSP00000325831.3:n.*410G>C
|
|
ENST00000333684.9:c.695+428G>C
|
ENSP00000328814.6:n.695+428G>C
|
|
ENST00000352909.7:c.721G>C
|
ENSP00000325951.3:p.Gly241Arg
|
|
ENST00000381168.7:c.*441G>C
|
ENSP00000370560.3:n.*441G>C
|
|
ENST00000381175.5:c.802G>C
|
ENSP00000370567.1:p.Gly268Arg
|
|
ENST00000381178.5:c.814G>C
|
ENSP00000370571.1:p.Gly272Arg
|
|
ENST00000412076.1:c.135+428G>C
|
|
|
ENST00000416223.5:c.136-239G>C
|
|
|
ENST00000469226.1:n.850G>C
|
|
|
ENST00000479437.5:n.270G>C
|
|
|
NM_000360.3:c.721G>C
|
NP_000351.2:p.Gly241Arg
|
|
NM_199292.2:c.814G>C
|
NP_954986.2:p.Gly272Arg
|
|
NM_199293.2:c.802G>C
|
NP_954987.2:p.Gly268Arg
|
|
XM_011520335.1:c.733G>C
|
XP_011518637.1:p.Gly245Arg
|
|
XM_011520335.2:c.733G>C
|
XP_011518637.1:p.Gly245Arg
|
|
NM_000360.4:c.721G>C
MANE Select
|
NP_000351.2:p.Gly241Arg
|
|
NM_199292.3:c.814G>C
|
NP_954986.2:p.Gly272Arg
|
|
NM_199293.3:c.802G>C
|
NP_954987.2:p.Gly268Arg
|
|