ENST00000225737.11:c.1940T>G
MANE Select
|
ENSP00000225737.6:p.Met647Arg
|
|
ENST00000225737.10:c.1940T>G
|
ENSP00000225737.6:p.Met647Arg
|
|
ENST00000395536.7:c.1766T>G
|
ENSP00000378907.3:p.Met589Arg
|
|
ENST00000578898.1:c.367T>G
|
|
|
NM_007202.3:c.1940T>G
|
NP_009133.2:p.Met647Arg
|
|
XM_006721431.2:c.1835-2992T>G
|
XP_006721494.1:n.1835-2992T>G
|
|
XM_006721432.2:c.1766T>G
|
XP_006721495.1:p.Met589Arg
|
|
XR_933969.1:n.1988T>G
|
|
|
XR_933970.1:n.1883-2992T>G
|
|
|
NM_001330152.1:c.1766T>G
|
NP_001317081.1:p.Met589Arg
|
|
XR_001752418.2:n.2052T>G
|
|
|
XR_933969.3:n.1971T>G
|
|
|
NM_007202.4:c.1940T>G
MANE Select
|
NP_009133.2:p.Met647Arg
|
|
NM_001330152.2:c.1766T>G
|
NP_001317081.1:p.Met589Arg
|
|