ENST00000352909.8:c.609G>T
MANE Select
|
ENSP00000325951.4:p.Arg203Ser
|
|
ENST00000324155.8:c.*298G>T
|
ENSP00000325831.3:n.*298G>T
|
|
ENST00000333684.9:c.609G>T
|
ENSP00000328814.6:p.Arg203Ser
|
|
ENST00000352909.7:c.609G>T
|
ENSP00000325951.3:p.Arg203Ser
|
|
ENST00000381168.7:c.*298G>T
|
ENSP00000370560.3:n.*298G>T
|
|
ENST00000381175.5:c.690G>T
|
ENSP00000370567.1:p.Arg230Ser
|
|
ENST00000381178.5:c.702G>T
|
ENSP00000370571.1:p.Arg234Ser
|
|
ENST00000412076.1:c.49G>T
|
|
|
ENST00000416223.5:c.49G>T
|
|
|
ENST00000469226.1:n.358G>T
|
|
|
NM_000360.3:c.609G>T
|
NP_000351.2:p.Arg203Ser
|
|
NM_199292.2:c.702G>T
|
NP_954986.2:p.Arg234Ser
|
|
NM_199293.2:c.690G>T
|
NP_954987.2:p.Arg230Ser
|
|
XM_011520335.1:c.621G>T
|
XP_011518637.1:p.Arg207Ser
|
|
XM_011520335.2:c.621G>T
|
XP_011518637.1:p.Arg207Ser
|
|
NM_000360.4:c.609G>T
MANE Select
|
NP_000351.2:p.Arg203Ser
|
|
NM_199292.3:c.702G>T
|
NP_954986.2:p.Arg234Ser
|
|
NM_199293.3:c.690G>T
|
NP_954987.2:p.Arg230Ser
|
|