ENST00000352909.8:c.1017G>C
MANE Select
|
ENSP00000325951.4:p.Leu339=
|
|
ENST00000324155.8:c.*706G>C
|
ENSP00000325831.3:n.*706G>C
|
|
ENST00000333684.9:c.735G>C
|
ENSP00000328814.6:p.Leu245=
|
|
ENST00000352909.7:c.1017G>C
|
ENSP00000325951.3:p.Leu339=
|
|
ENST00000381168.7:c.*737G>C
|
ENSP00000370560.3:n.*737G>C
|
|
ENST00000381175.5:c.1098G>C
|
ENSP00000370567.1:p.Leu366=
|
|
ENST00000381178.5:c.1110G>C
|
ENSP00000370571.1:p.Leu370=
|
|
ENST00000412076.1:c.175G>C
|
|
|
ENST00000416223.5:c.311G>C
|
|
|
ENST00000461172.1:n.182G>C
|
|
|
ENST00000479437.5:n.566G>C
|
|
|
NM_000360.3:c.1017G>C
|
NP_000351.2:p.Leu339=
|
|
NM_199292.2:c.1110G>C
|
NP_954986.2:p.Leu370=
|
|
NM_199293.2:c.1098G>C
|
NP_954987.2:p.Leu366=
|
|
XM_011520335.1:c.1029G>C
|
XP_011518637.1:p.Leu343=
|
|
XM_011520335.2:c.1029G>C
|
XP_011518637.1:p.Leu343=
|
|
NM_000360.4:c.1017G>C
MANE Select
|
NP_000351.2:p.Leu339=
|
|
NM_199292.3:c.1110G>C
|
NP_954986.2:p.Leu370=
|
|
NM_199293.3:c.1098G>C
|
NP_954987.2:p.Leu366=
|
|