NM_006221.4:c.99G=
MANE Select
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NP_006212.1:p.Gln33=
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ENST00000247970.9:c.99G=
MANE Select
|
ENSP00000247970.5:p.Gln33=
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NM_006221.3:c.99G= , LRG_847t1:c.99G=
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NP_006212.1:p.Gln33=
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NR_038422.2:n.290G=
|
|
NR_038422.3:n.179G=
|
|
NR_038830.1:n.290G=
|
|
NR_038830.2:n.179G=
|
|
ENST00000247970.8:c.99G=
|
ENSP00000247970.4:p.Gln33=
|
ENST00000380889.6:n.1132G=
|
|
ENST00000585442.5:n.237G=
|
|
ENST00000586025.5:n.3146G=
|
|
ENST00000586352.5:c.162G=
|
|
ENST00000587625.5:c.99G=
|
ENSP00000466656.1:p.Gln33=
|
ENST00000588695.5:c.99G=
|
ENSP00000466962.1:p.Gln33=
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ENST00000589058.5:n.128G=
|
|
ENST00000590540.5:n.157G=
|
|
XM_011528068.1:c.114G=
|
XP_011526370.1:p.Gln38=
|
XM_011528068.2:c.114G=
|
XP_011526370.1:p.Gln38=
|