ENST00000593677.2:c.1575T=
|
|
|
ENST00000688602.1:c.2972T=
|
|
|
ENST00000689936.1:c.2944T=
|
|
|
ENST00000359596.8:c.14639T=
MANE Select
|
ENSP00000352608.2:p.Met4880=
|
|
ENST00000355481.8:c.14624T=
|
ENSP00000347667.3:p.Met4875=
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ENST00000359596.7:c.14639T=
|
ENSP00000352608.2:p.Met4880=
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|
ENST00000360985.7:c.14621T=
|
ENSP00000354254.4:p.Met4874=
|
|
NM_000540.2:c.14639T= , LRG_766t1:c.14639T=
|
NP_000531.2:p.Met4880=
|
|
NM_001042723.1:c.14624T=
|
NP_001036188.1:p.Met4875=
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XM_006723317.1:c.14621T=
|
XP_006723380.1:p.Met4874=
|
|
XM_006723319.1:c.14606T=
|
XP_006723382.1:p.Met4869=
|
|
XM_011527204.1:c.14636T=
|
XP_011525506.1:p.Met4879=
|
|
XM_011527205.1:c.14552T=
|
XP_011525507.1:p.Met4851=
|
|
XM_006723317.2:c.14621T=
|
XP_006723380.1:p.Met4874=
|
|
XM_006723319.2:c.14606T=
|
XP_006723382.1:p.Met4869=
|
|
XM_011527205.2:c.14552T=
|
XP_011525507.1:p.Met4851=
|
|
NM_000540.3:c.14639T=
MANE Select
|
NP_000531.2:p.Met4880=
|
|
NM_001042723.2:c.14624T=
|
NP_001036188.1:p.Met4875=
|
|