ENST00000352909.8:c.836T>A
MANE Select
|
ENSP00000325951.4:p.Leu279Gln
|
|
ENST00000324155.8:c.*525T>A
|
ENSP00000325831.3:n.*525T>A
|
|
ENST00000333684.9:c.696-343T>A
|
ENSP00000328814.6:n.696-343T>A
|
|
ENST00000352909.7:c.836T>A
|
ENSP00000325951.3:p.Leu279Gln
|
|
ENST00000381168.7:c.*556T>A
|
ENSP00000370560.3:n.*556T>A
|
|
ENST00000381175.5:c.917T>A
|
ENSP00000370567.1:p.Leu306Gln
|
|
ENST00000381178.5:c.929T>A
|
ENSP00000370571.1:p.Leu310Gln
|
|
ENST00000412076.1:c.136-343T>A
|
|
|
ENST00000416223.5:c.136-124T>A
|
|
|
ENST00000479437.5:n.385T>A
|
|
|
NM_000360.3:c.836T>A
|
NP_000351.2:p.Leu279Gln
|
|
NM_199292.2:c.929T>A
|
NP_954986.2:p.Leu310Gln
|
|
NM_199293.2:c.917T>A
|
NP_954987.2:p.Leu306Gln
|
|
XM_011520335.1:c.848T>A
|
XP_011518637.1:p.Leu283Gln
|
|
XM_011520335.2:c.848T>A
|
XP_011518637.1:p.Leu283Gln
|
|
NM_000360.4:c.836T>A
MANE Select
|
NP_000351.2:p.Leu279Gln
|
|
NM_199292.3:c.929T>A
|
NP_954986.2:p.Leu310Gln
|
|
NM_199293.3:c.917T>A
|
NP_954987.2:p.Leu306Gln
|
|