ENST00000389048.8:c.3528C>G
MANE Select
|
ENSP00000373700.3:p.His1176Gln
|
|
ENST00000431873.6:c.755C>G
|
|
|
ENST00000638605.1:n.405C>G
|
|
|
ENST00000642122.1:c.324C>G
|
ENSP00000493203.1:p.His108Gln
|
|
ENST00000389048.7:c.3528C>G
|
ENSP00000373700.3:p.His1176Gln
|
|
ENST00000431873.5:c.408C>G
|
ENSP00000414027.2:p.His136Gln
|
|
ENST00000618119.4:c.2397C>G
|
ENSP00000482733.1:p.His799Gln
|
|
NM_004304.4:c.3528C>G
|
NP_004295.2:p.His1176Gln
|
|
NM_001353765.1:c.324C>G
|
NP_001340694.1:p.His108Gln
|
|
XM_024452778.1:c.681C>G
|
XP_024308546.1:p.His227Gln
|
|
XM_024452779.1:c.324C>G
|
XP_024308547.1:p.His108Gln
|
|
NM_004304.5:c.3528C>G
MANE Select
|
NP_004295.2:p.His1176Gln
|
|
NM_001353765.2:c.324C>G
|
NP_001340694.1:p.His108Gln
|
|