ENST00000264071.7:c.725T>C
MANE Select
|
ENSP00000264071.1:p.Phe242Ser
|
|
ENST00000264071.6:c.725T>C
|
ENSP00000264071.1:p.Phe242Ser
|
|
ENST00000540257.5:c.725T>C
|
ENSP00000443590.1:p.Phe242Ser
|
|
ENST00000594276.5:c.413T>C
|
ENSP00000472481.1:p.Phe138Ser
|
|
NM_001289123.1:c.878T>C
|
NP_001276052.1:p.Phe293Ser
|
|
NM_001289127.1:c.860T>C
|
NP_001276056.1:p.Phe287Ser
|
|
NM_001289129.1:c.725T>C
|
NP_001276058.1:p.Phe242Ser
|
|
NM_001289130.1:c.509T>C
|
NP_001276059.1:p.Phe170Ser
|
|
NM_001289131.1:c.509T>C
|
NP_001276060.1:p.Phe170Ser
|
|
NM_006087.3:c.725T>C
|
NP_006078.2:p.Phe242Ser
|
|
NM_006087.4:c.725T>C
MANE Select
|
NP_006078.2:p.Phe242Ser
|
|
NM_001289123.2:c.878T>C
|
NP_001276052.1:p.Phe293Ser
|
|
NM_001289127.2:c.860T>C
|
NP_001276056.1:p.Phe287Ser
|
|
NM_001289129.2:c.725T>C
|
NP_001276058.1:p.Phe242Ser
|
|
NM_001289130.2:c.509T>C
|
NP_001276059.1:p.Phe170Ser
|
|
NM_001289131.2:c.509T>C
|
NP_001276060.1:p.Phe170Ser
|
|