ENST00000248633.9:c.1152A=
MANE Select
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ENSP00000248633.4:p.Leu384=
|
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ENST00000248633.8:c.1152A=
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ENSP00000248633.4:p.Leu384=
|
|
ENST00000422866.1:c.53A=
|
|
|
ENST00000428214.5:c.1152A=
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ENSP00000394413.1:p.Leu384=
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|
ENST00000438045.5:c.274-3396A=
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ENSP00000410438.1:n.274-3396A=
|
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ENST00000484913.5:n.1191A=
|
|
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NM_000466.2:c.1152A=
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NP_000457.1:p.Leu384=
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|
NM_001282677.1:c.1152A=
|
NP_001269606.1:p.Leu384=
|
|
NM_001282678.1:c.528A=
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NP_001269607.1:p.Leu176=
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|
XR_242246.3:n.1248A=
|
|
|
XM_017012319.2:c.-515A=
|
XP_016867808.1:n.-515A=
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|
XR_001744808.2:n.262A=
|
|
|
XR_242246.5:n.1199A=
|
|
|
NM_000466.3:c.1152A=
MANE Select
|
NP_000457.1:p.Leu384=
|
|
NM_001282677.2:c.1152A=
|
NP_001269606.1:p.Leu384=
|
|
NM_001282678.2:c.528A=
|
NP_001269607.1:p.Leu176=
|
|