ENST00000229307.9:c.288G>T
MANE Select
|
ENSP00000229307.4:p.Gln96His
|
|
ENST00000229307.8:c.288G>T
|
ENSP00000229307.4:p.Gln96His
|
|
ENST00000526286.1:c.288G>T
|
ENSP00000435288.1:p.Gln96His
|
|
ENST00000526434.2:n.432G>T
|
|
|
ENST00000541267.5:c.216G>T
|
ENSP00000444434.1:p.Gln72His
|
|
NM_001297698.1:c.288G>T
|
NP_001284627.1:p.Gln96His
|
|
NM_024865.3:c.288G>T
|
NP_079141.2:p.Gln96His
|
|
XM_011520850.1:c.288G>T
|
XP_011519152.1:p.Gln96His
|
|
XM_011520851.1:c.216G>T
|
XP_011519153.1:p.Gln72His
|
|
XM_011520852.1:c.-85G>T
|
XP_011519154.1:n.-85G>T
|
|
NM_024865.4:c.288G>T
MANE Select
|
NP_079141.2:p.Gln96His
|
|
NM_001297698.2:c.288G>T
|
NP_001284627.1:p.Gln96His
|
|