ENST00000248633.9:c.2335T=
MANE Select
|
ENSP00000248633.4:p.Phe779=
|
|
ENST00000248633.8:c.2335T=
|
ENSP00000248633.4:p.Phe779=
|
|
ENST00000428214.5:c.2164T=
|
ENSP00000394413.1:p.Phe722=
|
|
ENST00000438045.5:c.1369T=
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ENSP00000410438.1:p.Phe457=
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|
ENST00000484913.5:n.2374T=
|
|
|
ENST00000496092.1:n.133T=
|
|
|
ENST00000496420.5:n.2011T=
|
|
|
NM_000466.2:c.2335T=
|
NP_000457.1:p.Phe779=
|
|
NM_001282677.1:c.2164T=
|
NP_001269606.1:p.Phe722=
|
|
NM_001282678.1:c.1711T=
|
NP_001269607.1:p.Phe571=
|
|
XM_005250433.3:c.586T=
|
XP_005250490.1:p.Phe196=
|
|
XR_242246.3:n.2431T=
|
|
|
XM_017012319.2:c.586T=
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XP_016867808.1:p.Phe196=
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|
XR_001744808.2:n.1362T=
|
|
|
XR_242246.5:n.2382T=
|
|
|
NM_000466.3:c.2335T=
MANE Select
|
NP_000457.1:p.Phe779=
|
|
NM_001282677.2:c.2164T=
|
NP_001269606.1:p.Phe722=
|
|
NM_001282678.2:c.1711T=
|
NP_001269607.1:p.Phe571=
|
|