ENST00000225737.11:c.1933G>C
MANE Select
|
ENSP00000225737.6:p.Asp645His
|
|
ENST00000225737.10:c.1933G>C
|
ENSP00000225737.6:p.Asp645His
|
|
ENST00000395536.7:c.1759G>C
|
ENSP00000378907.3:p.Asp587His
|
|
ENST00000578898.1:c.360G>C
|
|
|
NM_007202.3:c.1933G>C
|
NP_009133.2:p.Asp645His
|
|
XM_006721431.2:c.1835-2999G>C
|
XP_006721494.1:n.1835-2999G>C
|
|
XM_006721432.2:c.1759G>C
|
XP_006721495.1:p.Asp587His
|
|
XR_933969.1:n.1981G>C
|
|
|
XR_933970.1:n.1883-2999G>C
|
|
|
NM_001330152.1:c.1759G>C
|
NP_001317081.1:p.Asp587His
|
|
XR_001752418.2:n.2045G>C
|
|
|
XR_933969.3:n.1964G>C
|
|
|
NM_007202.4:c.1933G>C
MANE Select
|
NP_009133.2:p.Asp645His
|
|
NM_001330152.2:c.1759G>C
|
NP_001317081.1:p.Asp587His
|
|