ENST00000542639.6:c.521T>G
|
ENSP00000440846.1:p.Met174Arg
|
|
ENST00000686683.1:c.230T>G
|
ENSP00000509063.1:p.Met77Arg
|
|
ENST00000686980.1:n.1052T>G
|
|
|
ENST00000688006.1:c.521T>G
|
ENSP00000510311.1:p.Met174Arg
|
|
ENST00000688859.1:n.476T>G
|
|
|
ENST00000689087.1:c.521T>G
|
ENSP00000508997.1:p.Met174Arg
|
|
ENST00000693128.1:c.815T>G
|
ENSP00000508493.1:p.Met272Arg
|
|
ENST00000338702.4:c.920T>G
MANE Select
|
ENSP00000340684.3:p.Met307Arg
|
|
ENST00000338702.3:c.920T>G
|
ENSP00000340684.3:p.Met307Arg
|
|
ENST00000542639.5:c.521T>G
|
ENSP00000440846.1:p.Met174Arg
|
|
NM_000240.3:c.920T>G
|
NP_000231.1:p.Met307Arg
|
|
NM_001270458.1:c.521T>G
|
NP_001257387.1:p.Met174Arg
|
|
NM_000240.4:c.920T>G
MANE Select
|
NP_000231.1:p.Met307Arg
|
|
NM_001270458.2:c.521T>G
|
NP_001257387.1:p.Met174Arg
|
|