ENST00000352909.8:c.1021G>T
MANE Select
|
ENSP00000325951.4:p.Asp341Tyr
|
|
ENST00000324155.8:c.*710G>T
|
ENSP00000325831.3:n.*710G>T
|
|
ENST00000333684.9:c.739G>T
|
ENSP00000328814.6:p.Asp247Tyr
|
|
ENST00000352909.7:c.1021G>T
|
ENSP00000325951.3:p.Asp341Tyr
|
|
ENST00000381168.7:c.*741G>T
|
ENSP00000370560.3:n.*741G>T
|
|
ENST00000381175.5:c.1102G>T
|
ENSP00000370567.1:p.Asp368Tyr
|
|
ENST00000381178.5:c.1114G>T
|
ENSP00000370571.1:p.Asp372Tyr
|
|
ENST00000412076.1:c.179G>T
|
|
|
ENST00000416223.5:c.315G>T
|
|
|
ENST00000461172.1:n.186G>T
|
|
|
ENST00000479437.5:n.570G>T
|
|
|
NM_000360.3:c.1021G>T
|
NP_000351.2:p.Asp341Tyr
|
|
NM_199292.2:c.1114G>T
|
NP_954986.2:p.Asp372Tyr
|
|
NM_199293.2:c.1102G>T
|
NP_954987.2:p.Asp368Tyr
|
|
XM_011520335.1:c.1033G>T
|
XP_011518637.1:p.Asp345Tyr
|
|
XM_011520335.2:c.1033G>T
|
XP_011518637.1:p.Asp345Tyr
|
|
NM_000360.4:c.1021G>T
MANE Select
|
NP_000351.2:p.Asp341Tyr
|
|
NM_199292.3:c.1114G>T
|
NP_954986.2:p.Asp372Tyr
|
|
NM_199293.3:c.1102G>T
|
NP_954987.2:p.Asp368Tyr
|
|