ENST00000352909.8:c.944G>A
MANE Select
|
ENSP00000325951.4:p.Arg315His
|
|
ENST00000324155.8:c.*633G>A
|
ENSP00000325831.3:n.*633G>A
|
|
ENST00000333684.9:c.696-117G>A
|
ENSP00000328814.6:n.696-117G>A
|
|
ENST00000352909.7:c.944G>A
|
ENSP00000325951.3:p.Arg315His
|
|
ENST00000381168.7:c.*664G>A
|
ENSP00000370560.3:n.*664G>A
|
|
ENST00000381175.5:c.1025G>A
|
ENSP00000370567.1:p.Arg342His
|
|
ENST00000381178.5:c.1037G>A
|
ENSP00000370571.1:p.Arg346His
|
|
ENST00000412076.1:c.136-117G>A
|
|
|
ENST00000416223.5:c.238G>A
|
|
|
ENST00000461172.1:n.109G>A
|
|
|
ENST00000479437.5:n.493G>A
|
|
|
NM_000360.3:c.944G>A
|
NP_000351.2:p.Arg315His
|
|
NM_199292.2:c.1037G>A
|
NP_954986.2:p.Arg346His
|
|
NM_199293.2:c.1025G>A
|
NP_954987.2:p.Arg342His
|
|
XM_011520335.1:c.956G>A
|
XP_011518637.1:p.Arg319His
|
|
XM_011520335.2:c.956G>A
|
XP_011518637.1:p.Arg319His
|
|
NM_000360.4:c.944G>A
MANE Select
|
NP_000351.2:p.Arg315His
|
|
NM_199292.3:c.1037G>A
|
NP_954986.2:p.Arg346His
|
|
NM_199293.3:c.1025G>A
|
NP_954987.2:p.Arg342His
|
|