ENST00000352909.8:c.891G>C
MANE Select
|
ENSP00000325951.4:p.Arg297=
|
|
ENST00000324155.8:c.*580G>C
|
ENSP00000325831.3:n.*580G>C
|
|
ENST00000333684.9:c.696-170G>C
|
ENSP00000328814.6:n.696-170G>C
|
|
ENST00000352909.7:c.891G>C
|
ENSP00000325951.3:p.Arg297=
|
|
ENST00000381168.7:c.*611G>C
|
ENSP00000370560.3:n.*611G>C
|
|
ENST00000381175.5:c.972G>C
|
ENSP00000370567.1:p.Arg324=
|
|
ENST00000381178.5:c.984G>C
|
ENSP00000370571.1:p.Arg328=
|
|
ENST00000412076.1:c.136-170G>C
|
|
|
ENST00000416223.5:c.185G>C
|
|
|
ENST00000461172.1:n.56G>C
|
|
|
ENST00000479437.5:n.440G>C
|
|
|
NM_000360.3:c.891G>C
|
NP_000351.2:p.Arg297=
|
|
NM_199292.2:c.984G>C
|
NP_954986.2:p.Arg328=
|
|
NM_199293.2:c.972G>C
|
NP_954987.2:p.Arg324=
|
|
XM_011520335.1:c.903G>C
|
XP_011518637.1:p.Arg301=
|
|
XM_011520335.2:c.903G>C
|
XP_011518637.1:p.Arg301=
|
|
NM_000360.4:c.891G>C
MANE Select
|
NP_000351.2:p.Arg297=
|
|
NM_199292.3:c.984G>C
|
NP_954986.2:p.Arg328=
|
|
NM_199293.3:c.972G>C
|
NP_954987.2:p.Arg324=
|
|