ENST00000496887.7:c.643G>A
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ENSP00000434560.2:p.Ala215Thr
|
|
ENST00000646564.2:c.478-10466G>A
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ENSP00000495806.2:n.478-10466G>A
|
|
ENST00000155840.12:c.904G>A
MANE Select
|
ENSP00000155840.2:p.Ala302Thr
|
|
ENST00000335475.6:c.523G>A
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ENSP00000334497.5:p.Ala175Thr
|
|
ENST00000646564.1:c.124-10466G>A
|
ENSP00000495806.1:n.124-10466G>A
|
|
ENST00000155840.9:c.904G>A
|
ENSP00000155840.2:p.Ala302Thr
|
|
ENST00000335475.5:c.523G>A
|
ENSP00000334497.5:p.Ala175Thr
|
|
NM_000218.2:c.904G>A , LRG_287t1:c.904G>A
|
NP_000209.2:p.Ala302Thr
|
|
NM_181798.1:c.523G>A , LRG_287t2:c.523G>A
|
NP_861463.1:p.Ala175Thr
|
|
NM_000218.3:c.904G>A
MANE Select
|
NP_000209.2:p.Ala302Thr
|
|