ENST00000285021.12:c.2399A>G
MANE Select
|
ENSP00000285021.8:p.His800Arg
|
|
ENST00000285021.11:c.2399A>G
|
ENSP00000285021.7:p.His800Arg
|
|
ENST00000427795.2:n.264A>G
|
|
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ENST00000476581.6:c.*1852A>G
|
ENSP00000424548.1:n.*1852A>G
|
|
NM_004628.4:c.2399A>G , LRG_472t1:c.2399A>G
|
NP_004619.3:p.His800Arg
|
|
NR_027299.1:n.2379A>G
|
|
|
XM_011534092.1:c.2399A>G
|
XP_011532394.1:p.His800Arg
|
|
NM_001354726.1:c.1820A>G
|
NP_001341655.1:p.His607Arg
|
|
NM_001354727.1:c.2393A>G
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NP_001341656.1:p.His798Arg
|
|
NM_001354729.1:c.2381A>G
|
NP_001341658.1:p.His794Arg
|
|
NM_001354730.1:c.2153A>G
|
NP_001341659.1:p.His718Arg
|
|
NR_148950.1:n.2342A>G
|
|
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NR_148951.1:n.2218A>G
|
|
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XR_001740256.2:n.2432A>G
|
|
|
XR_002959580.1:n.2432A>G
|
|
|
XR_002959581.1:n.4049A>G
|
|
|
NM_001354727.2:c.2393A>G
|
NP_001341656.1:p.His798Arg
|
|
NM_004628.5:c.2399A>G
MANE Select
|
NP_004619.3:p.His800Arg
|
|
NR_148950.2:n.2271A>G
|
|
|
NR_148951.2:n.2147A>G
|
|
|
NM_001354726.2:c.1820A>G
|
NP_001341655.1:p.His607Arg
|
|
NM_001354729.2:c.2381A>G
|
NP_001341658.1:p.His794Arg
|
|
NM_001354730.2:c.2153A>G
|
NP_001341659.1:p.His718Arg
|
|