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ENST00000689481.1:c.*1001A=
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ENST00000690625.1:n.2360A=
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ENSP00000510712.1:n.*1176A=
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ENST00000691724.1:c.*281A=
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ENSP00000509255.1:n.*281A=
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ENST00000691888.1:c.216A=
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ENST00000691899.1:c.1324A=
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ENSP00000508763.1:p.Met442=
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ENST00000692069.1:n.1890A=
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ENST00000692093.1:c.1225A=
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ENST00000692311.1:n.2148A=
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ENST00000693705.1:c.*1001A=
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ENSP00000510697.1:n.*1001A=
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ENST00000251849.9:c.1324A=
MANE Select
|
ENSP00000251849.4:p.Met442=
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ENST00000442415.7:c.1384A=
|
ENSP00000401888.2:p.Met462=
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ENST00000494557.1:n.340A=
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NM_002880.3:c.1324A= , LRG_413t1:c.1324A=
|
NP_002871.1:p.Met442=
|
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XM_005265355.1:c.1324A=
|
XP_005265412.1:p.Met442=
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XM_005265357.1:c.1225A=
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XP_005265414.1:p.Met409=
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XM_005265358.3:c.1081A=
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XP_005265415.1:p.Met361=
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XM_005265359.3:c.982A=
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XP_005265416.1:p.Met328=
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XM_005265360.1:c.1324A=
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XP_005265417.1:p.Met442=
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XM_011533974.1:c.1324A=
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XP_011532276.1:p.Met442=
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XM_011533975.1:c.1081A=
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XP_011532277.1:p.Met361=
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NM_001354689.1:c.1384A=
|
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NM_001354690.1:c.1324A=
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NP_001341619.1:p.Met442=
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NM_001354691.1:c.1081A=
|
NP_001341620.1:p.Met361=
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NM_001354692.1:c.1081A=
|
NP_001341621.1:p.Met361=
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NM_001354693.1:c.1225A=
|
NP_001341622.1:p.Met409=
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NM_001354694.1:c.1141A=
|
NP_001341623.1:p.Met381=
|
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|
NM_001354695.1:c.982A=
|
NP_001341624.1:p.Met328=
|
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NR_148940.1:n.1852A=
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NR_148941.1:n.1798A=
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NR_148942.1:n.1737A=
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XM_011533974.3:c.1324A=
|
XP_011532276.1:p.Met442=
|
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|
XM_017006966.1:c.1225A=
|
XP_016862455.1:p.Met409=
|
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|
NM_001354689.3:c.1384A=
|
NP_001341618.1:p.Met462=
|
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|
NM_001354690.2:c.1324A=
|
NP_001341619.1:p.Met442=
|
|
|
NM_001354691.2:c.1081A=
|
NP_001341620.1:p.Met361=
|
|
|
NM_001354692.2:c.1081A=
|
NP_001341621.1:p.Met361=
|
|
|
NM_001354693.2:c.1225A=
|
NP_001341622.1:p.Met409=
|
|
|
NM_001354694.2:c.1141A=
|
NP_001341623.1:p.Met381=
|
|
|
NM_001354695.2:c.982A=
|
NP_001341624.1:p.Met328=
|
|
|
NR_148940.2:n.1768A=
|
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NR_148941.2:n.1714A=
|
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|
NR_148942.2:n.1653A=
|
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NM_001354690.3:c.1324A=
|
NP_001341619.1:p.Met442=
|
|
|
NM_001354691.3:c.1081A=
|
NP_001341620.1:p.Met361=
|
|
|
NM_001354692.3:c.1081A=
|
NP_001341621.1:p.Met361=
|
|
|
NM_001354693.3:c.1225A=
|
NP_001341622.1:p.Met409=
|
|
|
NM_001354694.3:c.1141A=
|
NP_001341623.1:p.Met381=
|
|
|
NM_001354695.3:c.982A=
|
NP_001341624.1:p.Met328=
|
|
|
NM_002880.4:c.1324A=
MANE Select
|
NP_002871.1:p.Met442=
|
|
|
NR_148940.3:n.1768A=
|
|
|
|
NR_148941.3:n.1714A=
|
|
|
|
NR_148942.3:n.1653A=
|
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|
