ENST00000398603.6:c.337-282G>A
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ENSP00000381604.1:n.337-282G>A
|
|
ENST00000398606.10:c.340G>A
MANE Select
|
ENSP00000381607.3:p.Ala114Thr
|
|
ENST00000646888.1:c.*56G>A
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ENSP00000494477.1:n.*56G>A
|
|
ENST00000398603.5:c.337-282G>A
|
ENSP00000381604.1:n.337-282G>A
|
|
ENST00000398606.7:c.340G>A
|
ENSP00000381607.3:p.Ala114Thr
|
|
ENST00000467591.1:n.451G>A
|
|
|
ENST00000494593.1:n.1135G>A
|
|
|
ENST00000495996.1:c.4G>A
|
ENSP00000484686.1:p.Ala2Thr
|
|
ENST00000498765.5:c.403G>A
|
|
|
NM_000852.3:c.340G>A , LRG_723t1:c.340G>A
|
NP_000843.1:p.Ala114Thr
|
|
NM_000852.4:c.340G>A
MANE Select
|
NP_000843.1:p.Ala114Thr
|
|