ENST00000262493.12:c.731T>G
MANE Select
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ENSP00000262493.6:p.Met244Arg
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ENST00000562316.6:c.398T>G
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ENSP00000457238.2:p.Met133Arg
|
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ENST00000564727.2:c.35T>G
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ENSP00000454971.2:p.Met12Arg
|
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ENST00000568375.2:c.116-3475T>G
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|
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ENST00000638185.1:n.946T>G
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|
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ENST00000638210.1:n.1031T>G
|
|
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ENST00000638705.1:c.731T>G
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ENSP00000491223.1:p.Met244Arg
|
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ENST00000638836.1:n.641T>G
|
|
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ENST00000639055.1:n.1452T>G
|
|
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ENST00000639251.1:n.632T>G
|
|
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ENST00000639268.1:c.366T>G
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|
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ENST00000639341.1:c.256T>G
|
|
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ENST00000639770.1:c.769T>G
|
ENSP00000491999.1:n.769T>G
|
|
ENST00000640390.1:n.661T>G
|
|
|
ENST00000640469.1:c.95T>G
|
ENSP00000491875.1:p.Met32Arg
|
|
ENST00000640560.1:n.507T>G
|
|
|
ENST00000640893.1:c.*129T>G
|
ENSP00000492677.1:n.*129T>G
|
|
ENST00000262493.10:c.731T>G
|
ENSP00000262493.6:p.Met244Arg
|
|
ENST00000568375.1:n.116-3475T>G
|
|
|
NM_020988.2:c.731T>G
|
NP_066268.1:p.Met244Arg
|
|
XM_011523003.1:c.605T>G
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XP_011521305.1:p.Met202Arg
|
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XM_011523003.3:c.605T>G
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XP_011521305.1:p.Met202Arg
|
|
NM_020988.3:c.731T>G
MANE Select
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NP_066268.1:p.Met244Arg
|
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