ENST00000352909.8:c.850G>C
MANE Select
|
ENSP00000325951.4:p.Gly284Arg
|
|
ENST00000324155.8:c.*539G>C
|
ENSP00000325831.3:n.*539G>C
|
|
ENST00000333684.9:c.696-211G>C
|
ENSP00000328814.6:n.696-211G>C
|
|
ENST00000352909.7:c.850G>C
|
ENSP00000325951.3:p.Gly284Arg
|
|
ENST00000381168.7:c.*570G>C
|
ENSP00000370560.3:n.*570G>C
|
|
ENST00000381175.5:c.931G>C
|
ENSP00000370567.1:p.Gly311Arg
|
|
ENST00000381178.5:c.943G>C
|
ENSP00000370571.1:p.Gly315Arg
|
|
ENST00000412076.1:c.136-211G>C
|
|
|
ENST00000416223.5:c.144G>C
|
|
|
ENST00000461172.1:n.15G>C
|
|
|
ENST00000479437.5:n.399G>C
|
|
|
NM_000360.3:c.850G>C
|
NP_000351.2:p.Gly284Arg
|
|
NM_199292.2:c.943G>C
|
NP_954986.2:p.Gly315Arg
|
|
NM_199293.2:c.931G>C
|
NP_954987.2:p.Gly311Arg
|
|
XM_011520335.1:c.862G>C
|
XP_011518637.1:p.Gly288Arg
|
|
XM_011520335.2:c.862G>C
|
XP_011518637.1:p.Gly288Arg
|
|
NM_000360.4:c.850G>C
MANE Select
|
NP_000351.2:p.Gly284Arg
|
|
NM_199292.3:c.943G>C
|
NP_954986.2:p.Gly315Arg
|
|
NM_199293.3:c.931G>C
|
NP_954987.2:p.Gly311Arg
|
|