ENST00000530449.2:n.116G=
|
|
|
ENST00000698254.1:c.1020G=
|
ENSP00000513629.1:p.Met340=
|
|
ENST00000698255.1:c.1440G=
|
ENSP00000513630.1:p.Met480=
|
|
ENST00000698256.1:c.957G=
|
|
|
ENST00000698257.1:n.909G=
|
|
|
ENST00000698258.1:n.626G=
|
|
|
ENST00000698259.1:n.392G=
|
|
|
ENST00000265686.8:c.1491G=
MANE Select
|
ENSP00000265686.3:p.Met497=
|
|
ENST00000265686.7:c.1491G=
|
ENSP00000265686.3:p.Met497=
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ENST00000525516.1:n.285G=
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ENST00000525724.5:n.803G=
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ENST00000528981.5:c.643G=
|
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|
ENST00000532635.5:c.843G=
|
ENSP00000434407.1:p.Met281=
|
|
ENST00000533005.5:n.604G=
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|
|
NM_006019.3:c.1491G=
|
NP_006010.2:p.Met497=
|
|
NM_006053.3:c.843G=
|
NP_006044.1:p.Met281=
|
|
XM_005273709.2:c.1491G=
|
XP_005273766.1:p.Met497=
|
|
XM_011544726.1:c.1491G=
|
XP_011543028.1:p.Met497=
|
|
XM_011544727.1:c.1491G=
|
XP_011543029.1:p.Met497=
|
|
XM_011544728.1:c.1491G=
|
XP_011543030.1:p.Met497=
|
|
XR_949754.1:n.1495G=
|
|
|
NM_001351059.1:c.597G=
|
NP_001337988.1:p.Met199=
|
|
XM_024448320.1:c.1584G=
|
XP_024304088.1:p.Met528=
|
|
XM_024448321.1:c.1584G=
|
XP_024304089.1:p.Met528=
|
|
XM_024448322.1:c.1584G=
|
XP_024304090.1:p.Met528=
|
|
XM_024448323.1:c.1584G=
|
XP_024304091.1:p.Met528=
|
|
XM_024448324.1:c.1584G=
|
XP_024304092.1:p.Met528=
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|
XR_001747721.2:n.1615G=
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|
XR_001747722.1:n.1628G=
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|
XR_001747723.2:n.1628G=
|
|
|
XR_002957115.1:n.1706G=
|
|
|
NM_006019.4:c.1491G=
MANE Select
|
NP_006010.2:p.Met497=
|
|
NM_001351059.2:c.597G=
|
NP_001337988.1:p.Met199=
|
|
NM_006053.4:c.843G=
|
NP_006044.1:p.Met281=
|
|