ENST00000285021.12:c.2236G>C
MANE Select
|
ENSP00000285021.8:p.Ala746Pro
|
|
ENST00000285021.11:c.2236G>C
|
ENSP00000285021.7:p.Ala746Pro
|
|
ENST00000427795.2:n.101G>C
|
|
|
ENST00000476581.6:c.*1689G>C
|
ENSP00000424548.1:n.*1689G>C
|
|
NM_004628.4:c.2236G>C , LRG_472t1:c.2236G>C
|
NP_004619.3:p.Ala746Pro
|
|
NR_027299.1:n.2216G>C
|
|
|
XM_011534092.1:c.2236G>C
|
XP_011532394.1:p.Ala746Pro
|
|
NM_001354726.1:c.1657G>C
|
NP_001341655.1:p.Ala553Pro
|
|
NM_001354727.1:c.2230G>C
|
NP_001341656.1:p.Ala744Pro
|
|
NM_001354729.1:c.2218G>C
|
NP_001341658.1:p.Ala740Pro
|
|
NM_001354730.1:c.1990G>C
|
NP_001341659.1:p.Ala664Pro
|
|
NR_148950.1:n.2179G>C
|
|
|
NR_148951.1:n.2055G>C
|
|
|
XR_001740256.2:n.2269G>C
|
|
|
XR_002959580.1:n.2269G>C
|
|
|
XR_002959581.1:n.3886G>C
|
|
|
NM_001354727.2:c.2230G>C
|
NP_001341656.1:p.Ala744Pro
|
|
NM_004628.5:c.2236G>C
MANE Select
|
NP_004619.3:p.Ala746Pro
|
|
NR_148950.2:n.2108G>C
|
|
|
NR_148951.2:n.1984G>C
|
|
|
NM_001354726.2:c.1657G>C
|
NP_001341655.1:p.Ala553Pro
|
|
NM_001354729.2:c.2218G>C
|
NP_001341658.1:p.Ala740Pro
|
|
NM_001354730.2:c.1990G>C
|
NP_001341659.1:p.Ala664Pro
|
|