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MANE Select
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ENST00000549941.7:c.1794G=
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XM_011538488.1:c.2052G=
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XP_011536790.1:p.Met684=
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NM_000289.6:c.2052G=
MANE Select
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NM_001166686.2:c.2265G=
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NP_001160158.1:p.Met755=
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NR_148955.1:n.3125G=
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XM_005268976.3:c.2361G=
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XM_017019469.1:c.2172G=
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XP_016874958.1:p.Met724=
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XM_024449020.1:c.2274G=
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XM_024449021.1:c.2151G=
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NM_001166687.2:c.2052G=
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NM_001166688.2:c.2052G=
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|
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|
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NM_001354742.2:c.2052G=
|
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|
|
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NM_001354743.2:c.2052G=
|
NP_001341672.1:p.Met684=
|
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NM_001354744.2:c.2052G=
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NP_001341673.1:p.Met684=
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NM_001354745.2:c.1965G=
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|
|
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NM_001354746.2:c.1926G=
|
NP_001341675.1:p.Met642=
|
|
|
NM_001354747.2:c.1902G=
|
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|
|
|
NM_001354748.2:c.1902G=
|
NP_001341677.1:p.Met634=
|
|
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NM_001363619.2:c.1959G=
|
NP_001350548.1:p.Met653=
|
|
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NR_148954.2:n.2355G=
|
|
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NR_148956.2:n.2281G=
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NR_148957.2:n.2510G=
|
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NR_148958.2:n.2258G=
|
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NR_148959.2:n.2184G=
|
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