ENST00000261304.7:c.635T>G
MANE Select
|
ENSP00000261304.2:p.Met212Arg
|
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ENST00000261304.6:c.635T>G
|
ENSP00000261304.2:p.Met212Arg
|
|
ENST00000393568.8:c.566T>G
|
ENSP00000377198.4:p.Met189Arg
|
|
ENST00000393569.6:c.557T>G
|
ENSP00000377199.2:p.Met186Arg
|
|
ENST00000474294.6:n.625T>G
|
|
|
ENST00000477716.3:n.390T>G
|
|
|
ENST00000544807.6:c.467T>G
|
ENSP00000437513.2:p.Met156Arg
|
|
ENST00000554916.5:n.514T>G
|
|
|
ENST00000555000.5:c.2T>G
|
ENSP00000450472.1:p.Met1Arg
|
|
ENST00000557316.5:c.*33T>G
|
ENSP00000452314.1:n.*33T>G
|
|
ENST00000622264.4:c.625T>G
|
|
|
NM_000153.3:c.635T>G
|
NP_000144.2:p.Met212Arg
|
|
NM_001201401.1:c.566T>G
|
NP_001188330.1:p.Met189Arg
|
|
NM_001201402.1:c.557T>G
|
NP_001188331.1:p.Met186Arg
|
|
XM_011536618.1:c.467T>G
|
XP_011534920.1:p.Met156Arg
|
|
XM_011536618.2:c.467T>G
|
XP_011534920.1:p.Met156Arg
|
|
NM_000153.4:c.635T>G
MANE Select
|
NP_000144.2:p.Met212Arg
|
|
NM_001201401.2:c.566T>G
|
NP_001188330.1:p.Met189Arg
|
|
NM_001201402.2:c.557T>G
|
NP_001188331.1:p.Met186Arg
|
|