ENST00000261304.7:c.1160T>G
MANE Select
|
ENSP00000261304.2:p.Met387Arg
|
|
ENST00000261304.6:c.1160T>G
|
ENSP00000261304.2:p.Met387Arg
|
|
ENST00000393568.8:c.1091T>G
|
ENSP00000377198.4:p.Met364Arg
|
|
ENST00000393569.6:c.1082T>G
|
ENSP00000377199.2:p.Met361Arg
|
|
ENST00000474294.6:n.1150T>G
|
|
|
ENST00000544807.6:c.992T>G
|
ENSP00000437513.2:p.Met331Arg
|
|
ENST00000555000.5:c.527T>G
|
ENSP00000450472.1:p.Met176Arg
|
|
ENST00000557316.5:c.*558T>G
|
ENSP00000452314.1:n.*558T>G
|
|
ENST00000557520.1:n.246T>G
|
|
|
ENST00000622264.4:c.1150T>G
|
|
|
NM_000153.3:c.1160T>G
|
NP_000144.2:p.Met387Arg
|
|
NM_001201401.1:c.1091T>G
|
NP_001188330.1:p.Met364Arg
|
|
NM_001201402.1:c.1082T>G
|
NP_001188331.1:p.Met361Arg
|
|
XM_011536618.1:c.992T>G
|
XP_011534920.1:p.Met331Arg
|
|
XM_011536618.2:c.992T>G
|
XP_011534920.1:p.Met331Arg
|
|
NM_000153.4:c.1160T>G
MANE Select
|
NP_000144.2:p.Met387Arg
|
|
NM_001201401.2:c.1091T>G
|
NP_001188330.1:p.Met364Arg
|
|
NM_001201402.2:c.1082T>G
|
NP_001188331.1:p.Met361Arg
|
|