ENST00000295497.13:c.303G>A
|
ENSP00000295497.7:p.Met101Ile
|
|
ENST00000444394.7:c.303G>A
|
ENSP00000411911.2:p.Met101Ile
|
|
ENST00000295497.12:c.303G>A
|
ENSP00000295497.7:p.Met101Ile
|
|
ENST00000409089.7:c.3G>A
|
ENSP00000386322.3:p.Met1Ile
|
|
ENST00000409900.9:c.678G>A
MANE Select
|
ENSP00000386741.4:p.Met226Ile
|
|
ENST00000413882.6:c.132G>A
|
ENSP00000410496.2:p.Met44Ile
|
|
ENST00000425395.6:c.*125G>A
|
ENSP00000405270.2:n.*125G>A
|
|
ENST00000443238.6:c.156G>A
|
ENSP00000409798.2:p.Met52Ile
|
|
ENST00000444394.6:c.303G>A
|
ENSP00000411911.2:p.Met101Ile
|
|
ENST00000444573.2:c.522G>A
|
ENSP00000392603.2:p.Met174Ile
|
|
ENST00000488080.6:n.321G>A
|
|
|
ENST00000650731.1:c.3G>A
|
ENSP00000499146.1:p.Met1Ile
|
|
ENST00000650938.1:c.202G>A
|
|
|
ENST00000651246.1:c.270G>A
|
ENSP00000498484.1:p.Met90Ile
|
|
ENST00000651373.1:c.192G>A
|
ENSP00000499174.1:p.Met64Ile
|
|
ENST00000651501.1:c.*125G>A
|
ENSP00000498894.1:n.*125G>A
|
|
ENST00000651717.1:c.253-11986G>A
|
ENSP00000499124.1:n.253-11986G>A
|
|
ENST00000652036.1:c.303G>A
|
ENSP00000499139.1:p.Met101Ile
|
|
ENST00000652154.1:n.576G>A
|
|
|
ENST00000295497.11:c.303G>A
|
ENSP00000295497.7:p.Met101Ile
|
|
ENST00000409089.6:c.3G>A
|
ENSP00000386322.2:p.Met1Ile
|
|
ENST00000409156.7:c.600G>A
|
ENSP00000386470.3:p.Met200Ile
|
|
ENST00000409597.5:c.126G>A
|
ENSP00000386469.1:p.Met42Ile
|
|
ENST00000409900.7:c.678G>A
|
ENSP00000386741.3:p.Met226Ile
|
|
ENST00000413882.5:c.132G>A
|
ENSP00000410496.1:p.Met44Ile
|
|
ENST00000425395.5:c.*229G>A
|
ENSP00000405270.1:n.*229G>A
|
|
ENST00000443238.5:c.156G>A
|
ENSP00000409798.1:p.Met52Ile
|
|
ENST00000444394.5:c.3G>A
|
ENSP00000411911.1:p.Met1Ile
|
|
ENST00000444573.1:c.303G>A
|
ENSP00000392603.1:p.Met101Ile
|
|
ENST00000485882.1:n.137G>A
|
|
|
ENST00000488080.5:n.529G>A
|
|
|
NM_001025201.3:c.600G>A
|
NP_001020372.2:p.Met200Ile
|
|
NM_001206602.1:c.303G>A
|
NP_001193531.1:p.Met101Ile
|
|
NM_001822.5:c.678G>A
|
NP_001813.1:p.Met226Ile
|
|
NR_038133.1:n.544G>A
|
|
|
NM_001025201.4:c.600G>A
|
NP_001020372.2:p.Met200Ile
|
|
NM_001206602.2:c.303G>A
|
NP_001193531.1:p.Met101Ile
|
|
NM_001371513.1:c.678G>A
|
NP_001358442.1:p.Met226Ile
|
|
NM_001371514.1:c.729G>A
|
NP_001358443.1:p.Met243Ile
|
|
NM_001822.7:c.678G>A
MANE Select
|
NP_001813.1:p.Met226Ile
|
|
NR_038133.2:n.546G>A
|
|
|