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ENST00000527846.7:n.1271G=
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ENST00000528667.7:c.1416G=
MANE Select
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ENSP00000436541.2:p.Met472=
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ENST00000531203.6:c.1224G=
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ENSP00000431975.2:p.Met408=
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|
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|
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|
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|
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|
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|
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|
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|
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|
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NM_001257360.1:c.1578G=
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NP_001244289.1:p.Met526=
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NM_001257361.1:c.1224G=
|
NP_001244290.1:p.Met408=
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NM_001308170.1:c.1353G=
|
NP_001295099.1:p.Met451=
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NM_004037.7:c.1578G=
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NP_004028.3:p.Met526=
|
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NM_139156.3:c.1335G=
|
NP_631895.1:p.Met445=
|
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NM_203404.1:c.1221G=
|
NP_981949.1:p.Met407=
|
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|
XM_011541247.1:c.1791G=
|
XP_011539549.1:p.Met597=
|
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|
XM_011541248.1:c.1782+156G=
|
XP_011539550.1:n.1782+156G=
|
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XR_946607.1:n.1814G=
|
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XM_024446431.1:c.1353G=
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XP_024302199.1:p.Met451=
|
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XM_024446432.1:c.1430+156G=
|
XP_024302200.1:n.1430+156G=
|
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XR_002956282.1:n.1989G=
|
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NM_001257360.2:c.1578G=
|
NP_001244289.1:p.Met526=
|
|
|
NM_001368809.2:c.1416G=
MANE Select
|
NP_001355738.1:p.Met472=
|
|
|
NM_004037.9:c.1416G=
|
NP_004028.4:p.Met472=
|
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|
NM_001257361.2:c.1224G=
|
NP_001244290.1:p.Met408=
|
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NM_139156.4:c.1335G=
|
NP_631895.1:p.Met445=
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