ENST00000450565.8:c.218C>T
MANE Select
|
ENSP00000411658.3:p.Ala73Val
|
|
ENST00000269200.5:n.216C>T
|
|
|
ENST00000450565.7:c.218C>T
|
ENSP00000411658.3:p.Ala73Val
|
|
ENST00000579794.1:c.218C>T
|
ENSP00000462647.1:p.Ala73Val
|
|
NM_001099733.1:c.218C>T
|
NP_001093203.1:p.Ala73Val
|
|
NM_001117.4:c.218C>T
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NP_001108.2:p.Ala73Val
|
|
XM_005258081.2:c.701C>T
|
XP_005258138.1:p.Ala234Val
|
|
XM_005258081.4:c.635C>T
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XP_005258138.2:p.Ala212Val
|
|
NM_001099733.2:c.218C>T
MANE Select
|
NP_001093203.1:p.Ala73Val
|
|
NM_001117.5:c.218C>T
|
NP_001108.2:p.Ala73Val
|
|