ENST00000285021.12:c.2182A>T
MANE Select
|
ENSP00000285021.8:p.Asn728Tyr
|
|
ENST00000285021.11:c.2182A>T
|
ENSP00000285021.7:p.Asn728Tyr
|
|
ENST00000427795.2:n.47A>T
|
|
|
ENST00000476581.6:c.*1635A>T
|
ENSP00000424548.1:n.*1635A>T
|
|
NM_004628.4:c.2182A>T , LRG_472t1:c.2182A>T
|
NP_004619.3:p.Asn728Tyr
|
|
NR_027299.1:n.2162A>T
|
|
|
XM_011534092.1:c.2182A>T
|
XP_011532394.1:p.Asn728Tyr
|
|
NM_001354726.1:c.1603A>T
|
NP_001341655.1:p.Asn535Tyr
|
|
NM_001354727.1:c.2176A>T
|
NP_001341656.1:p.Asn726Tyr
|
|
NM_001354729.1:c.2164A>T
|
NP_001341658.1:p.Asn722Tyr
|
|
NM_001354730.1:c.1936A>T
|
NP_001341659.1:p.Asn646Tyr
|
|
NR_148950.1:n.2125A>T
|
|
|
NR_148951.1:n.2001A>T
|
|
|
XR_001740256.2:n.2215A>T
|
|
|
XR_002959580.1:n.2215A>T
|
|
|
XR_002959581.1:n.3832A>T
|
|
|
NM_001354727.2:c.2176A>T
|
NP_001341656.1:p.Asn726Tyr
|
|
NM_004628.5:c.2182A>T
MANE Select
|
NP_004619.3:p.Asn728Tyr
|
|
NR_148950.2:n.2054A>T
|
|
|
NR_148951.2:n.1930A>T
|
|
|
NM_001354726.2:c.1603A>T
|
NP_001341655.1:p.Asn535Tyr
|
|
NM_001354729.2:c.2164A>T
|
NP_001341658.1:p.Asn722Tyr
|
|
NM_001354730.2:c.1936A>T
|
NP_001341659.1:p.Asn646Tyr
|
|