ENST00000559133.6:c.5803G>A
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ENSP00000453958.2:p.Ala1935Thr
|
|
ENST00000674301.2:c.5803G>A
|
ENSP00000501333.2:p.Ala1935Thr
|
|
ENST00000684448.1:n.4477G>A
|
|
|
ENST00000316623.10:c.5803G>A
MANE Select
|
ENSP00000325527.5:p.Ala1935Thr
|
|
ENST00000674301.1:c.802G>A
|
ENSP00000501333.1:p.Ala268Thr
|
|
ENST00000316623.9:c.5803G>A
|
ENSP00000325527.5:p.Ala1935Thr
|
|
ENST00000537463.6:c.*1566G>A
|
ENSP00000440294.2:n.*1566G>A
|
|
ENST00000559133.5:c.1110G>A
|
|
|
NM_000138.4:c.5803G>A , LRG_778t1:c.5803G>A
|
NP_000129.3:p.Ala1935Thr
|
|
NM_000138.5:c.5803G>A
MANE Select
|
NP_000129.3:p.Ala1935Thr
|
|