ENST00000285021.12:c.1864G>T
MANE Select
|
ENSP00000285021.8:p.Asp622Tyr
|
|
ENST00000285021.11:c.1864G>T
|
ENSP00000285021.7:p.Asp622Tyr
|
|
ENST00000476581.6:c.*1317G>T
|
ENSP00000424548.1:n.*1317G>T
|
|
NM_004628.4:c.1864G>T , LRG_472t1:c.1864G>T
|
NP_004619.3:p.Asp622Tyr
|
|
NR_027299.1:n.1844G>T
|
|
|
XM_011534092.1:c.1864G>T
|
XP_011532394.1:p.Asp622Tyr
|
|
XM_011534093.1:c.1864G>T
|
XP_011532395.1:p.Asp622Tyr
|
|
NM_001354726.1:c.1285G>T
|
NP_001341655.1:p.Asp429Tyr
|
|
NM_001354727.1:c.1864G>T
|
NP_001341656.1:p.Asp622Tyr
|
|
NM_001354729.1:c.1846G>T
|
NP_001341658.1:p.Asp616Tyr
|
|
NM_001354730.1:c.1626+238G>T
|
NP_001341659.1:n.1626+238G>T
|
|
NR_148950.1:n.1968G>T
|
|
|
NR_148951.1:n.1844G>T
|
|
|
XR_001740256.2:n.1897G>T
|
|
|
XR_002959580.1:n.1897G>T
|
|
|
XR_002959581.1:n.1897G>T
|
|
|
NM_001354727.2:c.1864G>T
|
NP_001341656.1:p.Asp622Tyr
|
|
NM_004628.5:c.1864G>T
MANE Select
|
NP_004619.3:p.Asp622Tyr
|
|
NR_148950.2:n.1897G>T
|
|
|
NR_148951.2:n.1773G>T
|
|
|
NM_001354726.2:c.1285G>T
|
NP_001341655.1:p.Asp429Tyr
|
|
NM_001354729.2:c.1846G>T
|
NP_001341658.1:p.Asp616Tyr
|
|
NM_001354730.2:c.1626+238G>T
|
NP_001341659.1:n.1626+238G>T
|
|