ENST00000585362.7:c.658A>G
|
ENSP00000473614.3:p.Met220Val
|
|
ENST00000593032.6:c.527A>G
|
ENSP00000465828.4:p.His176Arg
|
|
ENST00000706713.1:c.541A>G
|
ENSP00000516510.1:p.Met181Val
|
|
ENST00000706714.1:c.527A>G
|
ENSP00000516511.1:p.His176Arg
|
|
ENST00000706715.1:c.163A>G
|
ENSP00000516512.1:p.Met55Val
|
|
ENST00000354171.13:c.547A>G
MANE Select
|
ENSP00000346103.7:p.Met183Val
|
|
ENST00000589115.6:c.522A>G
|
ENSP00000466872.3:p.Pro174=
|
|
ENST00000354171.12:c.547A>G
|
ENSP00000346103.7:p.Met183Val
|
|
ENST00000585480.1:c.280A>G
|
ENSP00000467900.1:p.Met94Val
|
|
ENST00000587648.5:c.427A>G
|
ENSP00000468349.1:p.Met143Val
|
|
ENST00000588919.5:c.488A>G
|
ENSP00000464989.3:p.His163Arg
|
|
ENST00000589115.5:c.522A>G
|
ENSP00000466872.2:p.Pro174=
|
|
ENST00000592940.2:n.918A>G
|
|
|
ENST00000611653.4:c.466A>G
|
ENSP00000483655.1:p.Met156Val
|
|
ENST00000616066.4:c.544A>G
|
ENSP00000485000.1:p.Met182Val
|
|
ENST00000622390.4:c.655A>G
|
ENSP00000477503.1:p.Met219Val
|
|
NM_001039847.2:c.569A>G
|
NP_001034936.1:p.His190Arg
|
|
NM_001039848.2:c.658A>G
|
NP_001034937.1:p.Met220Val
|
|
NM_002085.4:c.547A>G
|
NP_002076.2:p.Met183Val
|
|
NM_001039848.3:c.658A>G
|
NP_001034937.1:p.Met220Val
|
|
NM_001039847.3:c.569A>G
|
NP_001034936.1:p.His190Arg
|
|
NM_001039848.4:c.658A>G
|
NP_001034937.1:p.Met220Val
|
|
NM_001367832.1:c.466A>G
|
NP_001354761.1:p.Met156Val
|
|
NM_002085.5:c.547A>G
MANE Select
|
NP_002076.2:p.Met183Val
|
|