ENST00000264071.7:c.721C>T
MANE Select
|
ENSP00000264071.1:p.Arg241Cys
|
|
ENST00000264071.6:c.721C>T
|
ENSP00000264071.1:p.Arg241Cys
|
|
ENST00000540257.5:c.721C>T
|
ENSP00000443590.1:p.Arg241Cys
|
|
ENST00000594276.5:c.409C>T
|
ENSP00000472481.1:p.Arg137Cys
|
|
NM_001289123.1:c.874C>T
|
NP_001276052.1:p.Arg292Cys
|
|
NM_001289127.1:c.856C>T
|
NP_001276056.1:p.Arg286Cys
|
|
NM_001289129.1:c.721C>T
|
NP_001276058.1:p.Arg241Cys
|
|
NM_001289130.1:c.505C>T
|
NP_001276059.1:p.Arg169Cys
|
|
NM_001289131.1:c.505C>T
|
NP_001276060.1:p.Arg169Cys
|
|
NM_006087.3:c.721C>T
|
NP_006078.2:p.Arg241Cys
|
|
NM_006087.4:c.721C>T
MANE Select
|
NP_006078.2:p.Arg241Cys
|
|
NM_001289123.2:c.874C>T
|
NP_001276052.1:p.Arg292Cys
|
|
NM_001289127.2:c.856C>T
|
NP_001276056.1:p.Arg286Cys
|
|
NM_001289129.2:c.721C>T
|
NP_001276058.1:p.Arg241Cys
|
|
NM_001289130.2:c.505C>T
|
NP_001276059.1:p.Arg169Cys
|
|
NM_001289131.2:c.505C>T
|
NP_001276060.1:p.Arg169Cys
|
|