ENST00000557334.6:c.223A>G
|
ENSP00000452512.1:p.Met75Val
|
|
ENST00000685328.1:c.562A>G
|
ENSP00000508921.1:p.Met188Val
|
|
ENST00000686877.1:c.*533A>G
|
ENSP00000510431.1:n.*533A>G
|
|
ENST00000687356.1:c.*260A>G
|
ENSP00000510511.1:n.*260A>G
|
|
ENST00000688228.1:n.1036A>G
|
|
|
ENST00000688940.1:c.562A>G
|
ENSP00000509238.1:p.Met188Val
|
|
ENST00000690406.1:c.365A>G
|
|
|
ENST00000690804.1:c.*523A>G
|
ENSP00000508568.1:n.*523A>G
|
|
ENST00000692768.1:c.364A>G
|
ENSP00000510254.1:p.Met122Val
|
|
ENST00000693229.1:c.487A>G
|
ENSP00000509223.1:p.Met163Val
|
|
ENST00000256078.10:c.*116A>G
MANE Plus Clinical
|
ENSP00000256078.5:n.*116A>G
|
|
ENST00000311936.8:c.562A>G
MANE Select
|
ENSP00000308495.3:p.Met188Val
|
|
ENST00000256078.8:c.*116A>G
|
ENSP00000256078.4:n.*116A>G
|
|
ENST00000311936.7:c.562A>G
|
ENSP00000308495.3:p.Met188Val
|
|
ENST00000557334.5:c.223A>G
|
ENSP00000452512.1:p.Met75Val
|
|
NM_004985.4:c.562A>G
|
NP_004976.2:p.Met188Val
|
|
NM_033360.3:c.*116A>G
|
NP_203524.1:n.*116A>G
|
|
XM_011520653.1:c.562A>G
|
XP_011518955.1:p.Met188Val
|
|
XM_011520653.3:c.562A>G
|
XP_011518955.1:p.Met188Val
|
|
NM_001369786.1:c.*116A>G
|
NP_001356715.1:n.*116A>G
|
|
NM_001369787.1:c.562A>G
|
NP_001356716.1:p.Met188Val
|
|
NM_004985.5:c.562A>G
MANE Select
|
NP_004976.2:p.Met188Val
|
|
NM_033360.4:c.*116A>G
MANE Plus Clinical
|
NP_203524.1:n.*116A>G
|
|