ENST00000593677.2:c.1865G=
|
|
|
ENST00000688602.1:c.3262G=
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|
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ENST00000689936.1:c.3234G=
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|
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ENST00000692547.1:n.322G=
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|
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ENST00000359596.8:c.14929G=
MANE Select
|
ENSP00000352608.2:p.Glu4977=
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ENST00000355481.8:c.14914G=
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ENSP00000347667.3:p.Glu4972=
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|
ENST00000359596.7:c.14929G=
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ENSP00000352608.2:p.Glu4977=
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|
ENST00000360985.7:c.14911G=
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ENSP00000354254.4:p.Glu4971=
|
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NM_000540.2:c.14929G= , LRG_766t1:c.14929G=
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NP_000531.2:p.Glu4977=
|
|
NM_001042723.1:c.14914G=
|
NP_001036188.1:p.Glu4972=
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|
XM_006723317.1:c.14911G=
|
XP_006723380.1:p.Glu4971=
|
|
XM_006723319.1:c.14896G=
|
XP_006723382.1:p.Glu4966=
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XM_011527204.1:c.14926G=
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XP_011525506.1:p.Glu4976=
|
|
XM_011527205.1:c.14842G=
|
XP_011525507.1:p.Glu4948=
|
|
XM_006723317.2:c.14911G=
|
XP_006723380.1:p.Glu4971=
|
|
XM_006723319.2:c.14896G=
|
XP_006723382.1:p.Glu4966=
|
|
XM_011527205.2:c.14842G=
|
XP_011525507.1:p.Glu4948=
|
|
NM_000540.3:c.14929G=
MANE Select
|
NP_000531.2:p.Glu4977=
|
|
NM_001042723.2:c.14914G=
|
NP_001036188.1:p.Glu4972=
|
|