ENST00000259216.6:c.558C>T
MANE Select
|
ENSP00000259216.5:p.Leu186=
|
|
ENST00000259216.4:c.558C>T
|
ENSP00000259216.4:p.Leu186=
|
|
ENST00000615342.4:c.443C>T
|
ENSP00000480526.1:p.Ser148Phe
|
|
ENST00000621673.4:c.333C>T
|
ENSP00000480843.1:p.Leu111=
|
|
NM_001270420.1:c.443C>T
|
NP_001257349.1:p.Ser148Phe
|
|
NM_001270421.1:c.333C>T
|
NP_001257350.1:p.Leu111=
|
|
NM_032545.3:c.558C>T
|
NP_115934.1:p.Leu186=
|
|
NM_032545.4:c.558C>T
MANE Select
|
NP_115934.1:p.Leu186=
|
|
NM_001270420.2:c.443C>T
|
NP_001257349.1:p.Ser148Phe
|
|
NM_001270421.2:c.333C>T
|
NP_001257350.1:p.Leu111=
|
|