ENST00000699485.1:c.986C>A
|
ENSP00000514396.1:p.Ala329Asp
|
|
ENST00000362057.4:c.2642C>A
MANE Select
|
ENSP00000354623.3:p.Ala881Asp
|
|
ENST00000674036.8:c.1615C>A
|
|
|
ENST00000674048.1:n.2523C>A
|
|
|
ENST00000265134.10:c.1493C>A
|
ENSP00000265134.6:p.Ala498Asp
|
|
ENST00000362057.3:c.2642C>A
|
ENSP00000354623.3:p.Ala881Asp
|
|
ENST00000374059.7:c.1589C>A
|
ENSP00000363172.3:p.Ala530Asp
|
|
NM_001083885.2:c.1493C>A
|
NP_001077354.2:p.Ala498Asp
|
|
NM_001173425.1:c.2639C>A
|
NP_001166896.1:p.Ala880Asp
|
|
NM_015404.3:c.2642C>A
|
NP_056219.3:p.Ala881Asp
|
|
XM_005251897.3:c.1979C>A
|
XP_005251954.2:p.Ala660Asp
|
|
XM_011518484.1:c.2675C>A
|
XP_011516786.1:p.Ala892Asp
|
|
XM_011518485.1:c.2675C>A
|
XP_011516787.1:p.Ala892Asp
|
|
XM_011518486.1:c.2672C>A
|
XP_011516788.1:p.Ala891Asp
|
|
XM_011518487.1:c.2549C>A
|
XP_011516789.1:p.Ala850Asp
|
|
XM_011518488.1:c.2432C>A
|
XP_011516790.1:p.Ala811Asp
|
|
XM_011518495.1:c.1352C>A
|
XP_011516797.1:p.Ala451Asp
|
|
NM_001346890.1:c.1589C>A
|
NP_001333819.1:p.Ala530Asp
|
|
XM_011518486.2:c.2672C>A
|
XP_011516788.1:p.Ala891Asp
|
|
XM_011518487.2:c.2549C>A
|
XP_011516789.1:p.Ala850Asp
|
|
XM_011518488.2:c.2432C>A
|
XP_011516790.1:p.Ala811Asp
|
|
NM_015404.4:c.2642C>A
MANE Select
|
NP_056219.3:p.Ala881Asp
|
|
NM_001173425.2:c.2639C>A
|
NP_001166896.1:p.Ala880Asp
|
|
NM_001083885.3:c.1493C>A
|
NP_001077354.2:p.Ala498Asp
|
|