ENST00000352909.8:c.1005C>G
MANE Select
|
ENSP00000325951.4:p.His335Gln
|
|
ENST00000324155.8:c.*694C>G
|
ENSP00000325831.3:n.*694C>G
|
|
ENST00000333684.9:c.723C>G
|
ENSP00000328814.6:p.His241Gln
|
|
ENST00000352909.7:c.1005C>G
|
ENSP00000325951.3:p.His335Gln
|
|
ENST00000381168.7:c.*725C>G
|
ENSP00000370560.3:n.*725C>G
|
|
ENST00000381175.5:c.1086C>G
|
ENSP00000370567.1:p.His362Gln
|
|
ENST00000381178.5:c.1098C>G
|
ENSP00000370571.1:p.His366Gln
|
|
ENST00000412076.1:c.163C>G
|
|
|
ENST00000416223.5:c.299C>G
|
|
|
ENST00000461172.1:n.170C>G
|
|
|
ENST00000479437.5:n.554C>G
|
|
|
NM_000360.3:c.1005C>G
|
NP_000351.2:p.His335Gln
|
|
NM_199292.2:c.1098C>G
|
NP_954986.2:p.His366Gln
|
|
NM_199293.2:c.1086C>G
|
NP_954987.2:p.His362Gln
|
|
XM_011520335.1:c.1017C>G
|
XP_011518637.1:p.His339Gln
|
|
XM_011520335.2:c.1017C>G
|
XP_011518637.1:p.His339Gln
|
|
NM_000360.4:c.1005C>G
MANE Select
|
NP_000351.2:p.His335Gln
|
|
NM_199292.3:c.1098C>G
|
NP_954986.2:p.His366Gln
|
|
NM_199293.3:c.1086C>G
|
NP_954987.2:p.His362Gln
|
|