ENST00000285021.12:c.2323A>T
MANE Select
|
ENSP00000285021.8:p.Asn775Tyr
|
|
ENST00000285021.11:c.2323A>T
|
ENSP00000285021.7:p.Asn775Tyr
|
|
ENST00000427795.2:n.188A>T
|
|
|
ENST00000476581.6:c.*1776A>T
|
ENSP00000424548.1:n.*1776A>T
|
|
NM_004628.4:c.2323A>T , LRG_472t1:c.2323A>T
|
NP_004619.3:p.Asn775Tyr
|
|
NR_027299.1:n.2303A>T
|
|
|
XM_011534092.1:c.2323A>T
|
XP_011532394.1:p.Asn775Tyr
|
|
NM_001354726.1:c.1744A>T
|
NP_001341655.1:p.Asn582Tyr
|
|
NM_001354727.1:c.2317A>T
|
NP_001341656.1:p.Asn773Tyr
|
|
NM_001354729.1:c.2305A>T
|
NP_001341658.1:p.Asn769Tyr
|
|
NM_001354730.1:c.2077A>T
|
NP_001341659.1:p.Asn693Tyr
|
|
NR_148950.1:n.2266A>T
|
|
|
NR_148951.1:n.2142A>T
|
|
|
XR_001740256.2:n.2356A>T
|
|
|
XR_002959580.1:n.2356A>T
|
|
|
XR_002959581.1:n.3973A>T
|
|
|
NM_001354727.2:c.2317A>T
|
NP_001341656.1:p.Asn773Tyr
|
|
NM_004628.5:c.2323A>T
MANE Select
|
NP_004619.3:p.Asn775Tyr
|
|
NR_148950.2:n.2195A>T
|
|
|
NR_148951.2:n.2071A>T
|
|
|
NM_001354726.2:c.1744A>T
|
NP_001341655.1:p.Asn582Tyr
|
|
NM_001354729.2:c.2305A>T
|
NP_001341658.1:p.Asn769Tyr
|
|
NM_001354730.2:c.2077A>T
|
NP_001341659.1:p.Asn693Tyr
|
|