ENST00000248633.9:c.2283A=
MANE Select
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ENSP00000248633.4:p.Ile761=
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ENST00000248633.8:c.2283A=
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ENSP00000248633.4:p.Ile761=
|
|
ENST00000428214.5:c.2112A=
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ENSP00000394413.1:p.Ile704=
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|
ENST00000438045.5:c.1317A=
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ENSP00000410438.1:p.Ile439=
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ENST00000484913.5:n.2322A=
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|
|
ENST00000496092.1:n.81A=
|
|
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ENST00000496420.5:n.1959A=
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NM_000466.2:c.2283A=
|
NP_000457.1:p.Ile761=
|
|
NM_001282677.1:c.2112A=
|
NP_001269606.1:p.Ile704=
|
|
NM_001282678.1:c.1659A=
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NP_001269607.1:p.Ile553=
|
|
XM_005250433.3:c.534A=
|
XP_005250490.1:p.Ile178=
|
|
XR_242246.3:n.2379A=
|
|
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XM_017012319.2:c.534A=
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XP_016867808.1:p.Ile178=
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|
XR_001744808.2:n.1310A=
|
|
|
XR_242246.5:n.2330A=
|
|
|
NM_000466.3:c.2283A=
MANE Select
|
NP_000457.1:p.Ile761=
|
|
NM_001282677.2:c.2112A=
|
NP_001269606.1:p.Ile704=
|
|
NM_001282678.2:c.1659A=
|
NP_001269607.1:p.Ile553=
|
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