ENST00000352909.8:c.820G>T
MANE Select
|
ENSP00000325951.4:p.Asp274Tyr
|
|
ENST00000324155.8:c.*509G>T
|
ENSP00000325831.3:n.*509G>T
|
|
ENST00000333684.9:c.696-359G>T
|
ENSP00000328814.6:n.696-359G>T
|
|
ENST00000352909.7:c.820G>T
|
ENSP00000325951.3:p.Asp274Tyr
|
|
ENST00000381168.7:c.*540G>T
|
ENSP00000370560.3:n.*540G>T
|
|
ENST00000381175.5:c.901G>T
|
ENSP00000370567.1:p.Asp301Tyr
|
|
ENST00000381178.5:c.913G>T
|
ENSP00000370571.1:p.Asp305Tyr
|
|
ENST00000412076.1:c.136-359G>T
|
|
|
ENST00000416223.5:c.136-140G>T
|
|
|
ENST00000469226.1:n.949G>T
|
|
|
ENST00000479437.5:n.369G>T
|
|
|
NM_000360.3:c.820G>T
|
NP_000351.2:p.Asp274Tyr
|
|
NM_199292.2:c.913G>T
|
NP_954986.2:p.Asp305Tyr
|
|
NM_199293.2:c.901G>T
|
NP_954987.2:p.Asp301Tyr
|
|
XM_011520335.1:c.832G>T
|
XP_011518637.1:p.Asp278Tyr
|
|
XM_011520335.2:c.832G>T
|
XP_011518637.1:p.Asp278Tyr
|
|
NM_000360.4:c.820G>T
MANE Select
|
NP_000351.2:p.Asp274Tyr
|
|
NM_199292.3:c.913G>T
|
NP_954986.2:p.Asp305Tyr
|
|
NM_199293.3:c.901G>T
|
NP_954987.2:p.Asp301Tyr
|
|