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ENSP00000509915.1:p.Met1593=
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ENST00000686826.1:n.1110G=
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ENST00000687016.1:c.4692G=
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ENSP00000510454.1:n.*2516G=
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ENST00000693591.1:n.3599G=
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ENST00000380817.8:c.4791G=
MANE Select
|
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ENST00000348911.10:c.4716G=
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ENSP00000252027.7:p.Met1572=
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XM_005261931.1:c.4794G=
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XM_011530709.1:c.4821G=
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XM_011530711.1:c.4818G=
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XR_938344.1:n.4911G=
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XM_005261935.2:c.4713G=
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XP_005261992.1:p.Met1571=
|
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XM_011530709.2:c.4821G=
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XM_017028905.2:c.4743G=
|
XP_016884394.1:p.Met1581=
|
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NM_002972.4:c.4791G=
MANE Select
|
NP_002963.2:p.Met1597=
|
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