ENST00000290866.10:c.2425A=
MANE Select
|
ENSP00000290866.4:p.Ile809=
|
|
ENST00000290863.10:c.703A=
|
ENSP00000290863.6:p.Ile235=
|
|
ENST00000290866.9:c.2425A=
|
ENSP00000290866.4:p.Ile809=
|
|
ENST00000413513.7:c.703A=
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ENSP00000392247.3:p.Ile235=
|
|
ENST00000428043.5:c.2425A=
|
ENSP00000397593.2:p.Ile809=
|
|
ENST00000577647.2:c.703A=
|
ENSP00000464149.1:p.Ile235=
|
|
ENST00000578839.5:c.*495A=
|
ENSP00000462110.2:n.*495A=
|
|
ENST00000579204.1:c.684A=
|
ENSP00000464629.1:n.684A=
|
|
ENST00000579314.5:c.*154A=
|
ENSP00000462599.1:n.*154A=
|
|
ENST00000582005.5:c.*345A=
|
ENSP00000462002.1:n.*345A=
|
|
ENST00000582761.1:c.193A=
|
ENSP00000462909.1:p.Ile65=
|
|
ENST00000584865.5:n.371A=
|
|
|
NM_000789.3:c.2425A=
|
NP_000780.1:p.Ile809=
|
|
NM_001178057.1:c.703A=
|
NP_001171528.1:p.Ile235=
|
|
NM_152830.2:c.703A=
|
NP_690043.1:p.Ile235=
|
|
XM_005257110.1:c.1876A=
|
XP_005257167.1:p.Ile626=
|
|
XM_006721737.2:c.763A=
|
XP_006721800.2:p.Ile255=
|
|
XM_006721737.3:c.763A=
|
XP_006721800.2:p.Ile255=
|
|
NM_000789.4:c.2425A=
MANE Select
|
NP_000780.1:p.Ile809=
|
|
NM_001178057.2:c.703A=
|
NP_001171528.1:p.Ile235=
|
|
NM_152830.3:c.703A=
|
NP_690043.1:p.Ile235=
|
|
NM_001382700.1:c.1858A=
|
NP_001369629.1:p.Ile620=
|
|
NM_001382701.1:c.1573A=
|
NP_001369630.1:p.Ile525=
|
|
NM_001382702.1:c.355A=
|
NP_001369631.1:p.Ile119=
|
|
NR_168483.1:n.803A=
|
|
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