ENST00000352909.8:c.878T>A
MANE Select
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ENSP00000325951.4:p.Leu293Gln
|
|
ENST00000324155.8:c.*567T>A
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ENSP00000325831.3:n.*567T>A
|
|
ENST00000333684.9:c.696-183T>A
|
ENSP00000328814.6:n.696-183T>A
|
|
ENST00000352909.7:c.878T>A
|
ENSP00000325951.3:p.Leu293Gln
|
|
ENST00000381168.7:c.*598T>A
|
ENSP00000370560.3:n.*598T>A
|
|
ENST00000381175.5:c.959T>A
|
ENSP00000370567.1:p.Leu320Gln
|
|
ENST00000381178.5:c.971T>A
|
ENSP00000370571.1:p.Leu324Gln
|
|
ENST00000412076.1:c.136-183T>A
|
|
|
ENST00000416223.5:c.172T>A
|
|
|
ENST00000461172.1:n.43T>A
|
|
|
ENST00000479437.5:n.427T>A
|
|
|
NM_000360.3:c.878T>A
|
NP_000351.2:p.Leu293Gln
|
|
NM_199292.2:c.971T>A
|
NP_954986.2:p.Leu324Gln
|
|
NM_199293.2:c.959T>A
|
NP_954987.2:p.Leu320Gln
|
|
XM_011520335.1:c.890T>A
|
XP_011518637.1:p.Leu297Gln
|
|
XM_011520335.2:c.890T>A
|
XP_011518637.1:p.Leu297Gln
|
|
NM_000360.4:c.878T>A
MANE Select
|
NP_000351.2:p.Leu293Gln
|
|
NM_199292.3:c.971T>A
|
NP_954986.2:p.Leu324Gln
|
|
NM_199293.3:c.959T>A
|
NP_954987.2:p.Leu320Gln
|
|