ENST00000368985.8:c.906C>T
MANE Select
|
ENSP00000357981.3:p.His302=
|
|
ENST00000448301.7:c.678C>T
|
ENSP00000408414.2:p.His226=
|
|
ENST00000472977.7:c.906C>T
|
ENSP00000475176.2:p.His302=
|
|
ENST00000483930.2:c.*100C>T
|
ENSP00000475812.2:n.*100C>T
|
|
ENST00000607427.2:c.906C>T
|
ENSP00000475557.2:p.His302=
|
|
ENST00000679512.1:c.803C>T
|
ENSP00000505113.1:p.Thr268Ile
|
|
ENST00000679898.1:c.633C>T
|
ENSP00000505326.1:p.His211=
|
|
ENST00000680288.1:c.756C>T
|
ENSP00000506001.1:p.His252=
|
|
ENST00000680311.1:c.637C>T
|
ENSP00000505020.1:p.Gln213Ter
|
|
ENST00000680471.1:c.*77C>T
|
ENSP00000506603.1:n.*77C>T
|
|
ENST00000680664.1:c.729C>T
|
ENSP00000506248.1:p.His243=
|
|
ENST00000680931.1:c.*256C>T
|
ENSP00000504934.1:n.*256C>T
|
|
ENST00000681357.1:n.296C>T
|
|
|
ENST00000681444.1:c.906C>T
|
ENSP00000505359.1:p.His302=
|
|
ENST00000368985.7:c.906C>T
|
ENSP00000357981.3:p.His302=
|
|
ENST00000448301.6:c.756C>T
|
ENSP00000408414.1:p.His252=
|
|
ENST00000472977.6:c.199C>T
|
|
|
ENST00000483930.1:c.454C>T
|
ENSP00000475812.1:n.454C>T
|
|
NM_001199739.1:c.756C>T
|
NP_001186668.1:p.His252=
|
|
NM_004079.4:c.906C>T
|
NP_004070.3:p.His302=
|
|
NM_004079.5:c.906C>T
MANE Select
|
NP_004070.3:p.His302=
|
|
NM_001199739.2:c.756C>T
|
NP_001186668.1:p.His252=
|
|