ENST00000366669.9:c.1890A>G
MANE Select
|
ENSP00000355629.4:p.Ile630Met
|
|
ENST00000366668.7:c.1887A>G
|
ENSP00000355628.3:p.Ile629Met
|
|
ENST00000366669.8:c.1890A>G
|
ENSP00000355629.4:p.Ile630Met
|
|
ENST00000468893.6:c.*1748A>G
|
ENSP00000476305.1:n.*1748A>G
|
|
ENST00000478710.1:n.149A>G
|
|
|
ENST00000490900.1:n.669A>G
|
|
|
ENST00000534989.1:c.1713A>G
|
ENSP00000440349.1:p.Ile571Met
|
|
NM_001145036.1:c.1887A>G
|
NP_001138508.1:p.Ile629Met
|
|
NM_007357.2:c.1890A>G
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NP_031383.1:p.Ile630Met
|
|
NM_007357.3:c.1890A>G
MANE Select
|
NP_031383.1:p.Ile630Met
|
|
NM_001145036.2:c.1887A>G
|
NP_001138508.1:p.Ile629Met
|
|