ENST00000593677.2:c.1577A=
|
|
|
ENST00000688602.1:c.2974A=
|
|
|
ENST00000689936.1:c.2946A=
|
|
|
ENST00000359596.8:c.14641A=
MANE Select
|
ENSP00000352608.2:p.Met4881=
|
|
ENST00000355481.8:c.14626A=
|
ENSP00000347667.3:p.Met4876=
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|
ENST00000359596.7:c.14641A=
|
ENSP00000352608.2:p.Met4881=
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|
ENST00000360985.7:c.14623A=
|
ENSP00000354254.4:p.Met4875=
|
|
NM_000540.2:c.14641A= , LRG_766t1:c.14641A=
|
NP_000531.2:p.Met4881=
|
|
NM_001042723.1:c.14626A=
|
NP_001036188.1:p.Met4876=
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|
XM_006723317.1:c.14623A=
|
XP_006723380.1:p.Met4875=
|
|
XM_006723319.1:c.14608A=
|
XP_006723382.1:p.Met4870=
|
|
XM_011527204.1:c.14638A=
|
XP_011525506.1:p.Met4880=
|
|
XM_011527205.1:c.14554A=
|
XP_011525507.1:p.Met4852=
|
|
XM_006723317.2:c.14623A=
|
XP_006723380.1:p.Met4875=
|
|
XM_006723319.2:c.14608A=
|
XP_006723382.1:p.Met4870=
|
|
XM_011527205.2:c.14554A=
|
XP_011525507.1:p.Met4852=
|
|
NM_000540.3:c.14641A=
MANE Select
|
NP_000531.2:p.Met4881=
|
|
NM_001042723.2:c.14626A=
|
NP_001036188.1:p.Met4876=
|
|