ENST00000352909.8:c.936G>T
MANE Select
|
ENSP00000325951.4:p.Gln312His
|
|
ENST00000324155.8:c.*625G>T
|
ENSP00000325831.3:n.*625G>T
|
|
ENST00000333684.9:c.696-125G>T
|
ENSP00000328814.6:n.696-125G>T
|
|
ENST00000352909.7:c.936G>T
|
ENSP00000325951.3:p.Gln312His
|
|
ENST00000381168.7:c.*656G>T
|
ENSP00000370560.3:n.*656G>T
|
|
ENST00000381175.5:c.1017G>T
|
ENSP00000370567.1:p.Gln339His
|
|
ENST00000381178.5:c.1029G>T
|
ENSP00000370571.1:p.Gln343His
|
|
ENST00000412076.1:c.136-125G>T
|
|
|
ENST00000416223.5:c.230G>T
|
|
|
ENST00000461172.1:n.101G>T
|
|
|
ENST00000479437.5:n.485G>T
|
|
|
NM_000360.3:c.936G>T
|
NP_000351.2:p.Gln312His
|
|
NM_199292.2:c.1029G>T
|
NP_954986.2:p.Gln343His
|
|
NM_199293.2:c.1017G>T
|
NP_954987.2:p.Gln339His
|
|
XM_011520335.1:c.948G>T
|
XP_011518637.1:p.Gln316His
|
|
XM_011520335.2:c.948G>T
|
XP_011518637.1:p.Gln316His
|
|
NM_000360.4:c.936G>T
MANE Select
|
NP_000351.2:p.Gln312His
|
|
NM_199292.3:c.1029G>T
|
NP_954986.2:p.Gln343His
|
|
NM_199293.3:c.1017G>T
|
NP_954987.2:p.Gln339His
|
|