ENST00000699485.1:c.1003G>A
|
ENSP00000514396.1:p.Ala335Thr
|
|
ENST00000362057.4:c.2659G>A
MANE Select
|
ENSP00000354623.3:p.Ala887Thr
|
|
ENST00000674036.8:c.1632G>A
|
|
|
ENST00000674048.1:n.2540G>A
|
|
|
ENST00000265134.10:c.1510G>A
|
ENSP00000265134.6:p.Ala504Thr
|
|
ENST00000362057.3:c.2659G>A
|
ENSP00000354623.3:p.Ala887Thr
|
|
ENST00000374059.7:c.1606G>A
|
ENSP00000363172.3:p.Ala536Thr
|
|
NM_001083885.2:c.1510G>A
|
NP_001077354.2:p.Ala504Thr
|
|
NM_001173425.1:c.2656G>A
|
NP_001166896.1:p.Ala886Thr
|
|
NM_015404.3:c.2659G>A
|
NP_056219.3:p.Ala887Thr
|
|
XM_005251897.3:c.1996G>A
|
XP_005251954.2:p.Ala666Thr
|
|
XM_011518484.1:c.2692G>A
|
XP_011516786.1:p.Ala898Thr
|
|
XM_011518485.1:c.2692G>A
|
XP_011516787.1:p.Ala898Thr
|
|
XM_011518486.1:c.2689G>A
|
XP_011516788.1:p.Ala897Thr
|
|
XM_011518487.1:c.2566G>A
|
XP_011516789.1:p.Ala856Thr
|
|
XM_011518488.1:c.2449G>A
|
XP_011516790.1:p.Ala817Thr
|
|
XM_011518495.1:c.1369G>A
|
XP_011516797.1:p.Ala457Thr
|
|
NM_001346890.1:c.1606G>A
|
NP_001333819.1:p.Ala536Thr
|
|
XM_011518486.2:c.2689G>A
|
XP_011516788.1:p.Ala897Thr
|
|
XM_011518487.2:c.2566G>A
|
XP_011516789.1:p.Ala856Thr
|
|
XM_011518488.2:c.2449G>A
|
XP_011516790.1:p.Ala817Thr
|
|
NM_015404.4:c.2659G>A
MANE Select
|
NP_056219.3:p.Ala887Thr
|
|
NM_001173425.2:c.2656G>A
|
NP_001166896.1:p.Ala886Thr
|
|
NM_001083885.3:c.1510G>A
|
NP_001077354.2:p.Ala504Thr
|
|