ENST00000248633.9:c.2028T=
MANE Select
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ENSP00000248633.4:p.His676=
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ENST00000248633.8:c.2028T=
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ENSP00000248633.4:p.His676=
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ENST00000428214.5:c.1900+1473T=
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ENSP00000394413.1:n.1900+1473T=
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ENST00000438045.5:c.1062T=
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ENSP00000410438.1:p.His354=
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ENST00000484913.5:n.2067T=
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|
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ENST00000496420.5:n.1704T=
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|
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NM_000466.2:c.2028T=
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NP_000457.1:p.His676=
|
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NM_001282677.1:c.1900+1473T=
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NP_001269606.1:n.1900+1473T=
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|
NM_001282678.1:c.1404T=
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NP_001269607.1:p.His468=
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XM_005250433.3:c.279T=
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XP_005250490.1:p.His93=
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|
XR_242246.3:n.2124T=
|
|
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XM_017012319.2:c.279T=
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XP_016867808.1:p.His93=
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|
XR_001744808.2:n.1055T=
|
|
|
XR_242246.5:n.2075T=
|
|
|
NM_000466.3:c.2028T=
MANE Select
|
NP_000457.1:p.His676=
|
|
NM_001282677.2:c.1900+1473T=
|
NP_001269606.1:n.1900+1473T=
|
|
NM_001282678.2:c.1404T=
|
NP_001269607.1:p.His468=
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