ENST00000394867.9:n.1537C>G
|
|
|
ENST00000688002.1:n.3249C>G
|
|
|
ENST00000688751.1:n.234C>G
|
|
|
ENST00000689792.1:n.1002C>G
|
|
|
ENST00000262948.10:c.1098C>G
MANE Select
|
ENSP00000262948.4:p.His366Gln
|
|
ENST00000262948.9:c.1098C>G
|
ENSP00000262948.3:p.His366Gln
|
|
ENST00000394867.8:c.807C>G
|
ENSP00000378336.1:p.His269Gln
|
|
ENST00000597263.5:n.283C>G
|
|
|
ENST00000599021.1:c.208C>G
|
|
|
ENST00000600584.5:n.2547C>G
|
|
|
ENST00000601786.5:n.1399C>G
|
|
|
NM_030662.3:c.1098C>G , LRG_750t1:c.1098C>G
|
NP_109587.1:p.His366Gln
|
|
XM_006722799.2:c.819C>G
|
XP_006722862.1:p.His273Gln
|
|
XM_011528133.1:c.528C>G
|
XP_011526435.1:p.His176Gln
|
|
NM_030662.4:c.1098C>G
MANE Select
|
NP_109587.1:p.His366Gln
|
|