ENST00000311907.10:c.494C>G
MANE Select
|
ENSP00000308541.5:p.Thr165Arg
|
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ENST00000311907.9:c.494C>G
|
ENSP00000308541.5:p.Thr165Arg
|
|
ENST00000442468.1:c.464C>G
|
ENSP00000387413.1:p.Thr155Arg
|
|
ENST00000490274.1:n.274C>G
|
|
|
ENST00000530231.5:c.494C>G
|
ENSP00000433907.1:p.Thr165Arg
|
|
NM_000506.3:c.494C>G
|
NP_000497.1:p.Thr165Arg
|
|
NM_000506.4:c.494C>G , LRG_551t1:c.494C>G
|
NP_000497.1:p.Thr165Arg
|
|
NM_001311257.1:c.446C>G
|
NP_001298186.1:p.Thr149Arg
|
|
XR_428840.2:n.538C>G
|
|
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XR_428840.4:n.529C>G
|
|
|
NM_000506.5:c.494C>G
MANE Select
|
NP_000497.1:p.Thr165Arg
|
|
NM_001311257.2:c.446C>G
|
NP_001298186.1:p.Thr149Arg
|
|