ENST00000691183.1:c.*305G>C
|
ENSP00000509954.1:n.*305G>C
|
|
ENST00000378842.8:c.717G>C
MANE Select
|
ENSP00000368119.4:p.Trp239Cys
|
|
ENST00000378842.7:c.717G>C
|
ENSP00000368119.3:p.Trp239Cys
|
|
ENST00000450095.6:c.390G>C
|
ENSP00000401956.2:p.Trp130Cys
|
|
ENST00000473506.6:c.*305G>C
|
ENSP00000432839.2:n.*305G>C
|
|
ENST00000473529.5:n.876G>C
|
|
|
ENST00000487381.5:n.1407G>C
|
|
|
ENST00000489643.6:n.797G>C
|
|
|
ENST00000554085.5:c.*461G>C
|
ENSP00000450419.1:n.*461G>C
|
|
ENST00000554550.5:c.*337G>C
|
ENSP00000451435.1:n.*337G>C
|
|
ENST00000554638.5:n.1189G>C
|
|
|
ENST00000555020.5:n.1178G>C
|
|
|
ENST00000555086.5:n.721G>C
|
|
|
ENST00000555754.1:n.62G>C
|
|
|
ENST00000556244.1:c.704G>C
|
|
|
ENST00000556278.1:c.432+335G>C
|
ENSP00000451792.1:n.432+335G>C
|
|
ENST00000557706.5:n.1279G>C
|
|
|
NM_000155.3:c.717G>C
|
NP_000146.2:p.Trp239Cys
|
|
NM_001258332.1:c.390G>C
|
NP_001245261.1:p.Trp130Cys
|
|
NM_000155.4:c.717G>C
MANE Select
|
NP_000146.2:p.Trp239Cys
|
|
NM_001258332.2:c.390G>C
|
NP_001245261.1:p.Trp130Cys
|
|