ENST00000248633.9:c.1155A=
MANE Select
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ENSP00000248633.4:p.Gln385=
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ENST00000248633.8:c.1155A=
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ENSP00000248633.4:p.Gln385=
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|
ENST00000422866.1:c.56A=
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|
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ENST00000428214.5:c.1155A=
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ENSP00000394413.1:p.Gln385=
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ENST00000438045.5:c.274-3393A=
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ENSP00000410438.1:n.274-3393A=
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ENST00000484913.5:n.1194A=
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|
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NM_000466.2:c.1155A=
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NP_000457.1:p.Gln385=
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NM_001282677.1:c.1155A=
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NP_001269606.1:p.Gln385=
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NM_001282678.1:c.531A=
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NP_001269607.1:p.Gln177=
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XR_242246.3:n.1251A=
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|
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XM_017012319.2:c.-512A=
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XP_016867808.1:n.-512A=
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XR_001744808.2:n.265A=
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|
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XR_242246.5:n.1202A=
|
|
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NM_000466.3:c.1155A=
MANE Select
|
NP_000457.1:p.Gln385=
|
|
NM_001282677.2:c.1155A=
|
NP_001269606.1:p.Gln385=
|
|
NM_001282678.2:c.531A=
|
NP_001269607.1:p.Gln177=
|
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