ENST00000691183.1:c.*408G>C
|
ENSP00000509954.1:n.*408G>C
|
|
ENST00000378842.8:c.820G>C
MANE Select
|
ENSP00000368119.4:p.Asp274His
|
|
ENST00000378842.7:c.820G>C
|
ENSP00000368119.3:p.Asp274His
|
|
ENST00000450095.6:c.493G>C
|
ENSP00000401956.2:p.Asp165His
|
|
ENST00000473506.6:c.*408G>C
|
ENSP00000432839.2:n.*408G>C
|
|
ENST00000489643.6:n.900G>C
|
|
|
ENST00000554085.5:c.*564G>C
|
ENSP00000450419.1:n.*564G>C
|
|
ENST00000554550.5:c.*440G>C
|
ENSP00000451435.1:n.*440G>C
|
|
ENST00000554638.5:n.1292G>C
|
|
|
ENST00000555020.5:n.1281G>C
|
|
|
ENST00000555086.5:n.824G>C
|
|
|
ENST00000555754.1:n.165G>C
|
|
|
ENST00000556244.1:c.807G>C
|
|
|
ENST00000556278.1:c.432+438G>C
|
ENSP00000451792.1:n.432+438G>C
|
|
ENST00000557706.5:n.1382G>C
|
|
|
NM_000155.3:c.820G>C
|
NP_000146.2:p.Asp274His
|
|
NM_001258332.1:c.493G>C
|
NP_001245261.1:p.Asp165His
|
|
NM_000155.4:c.820G>C
MANE Select
|
NP_000146.2:p.Asp274His
|
|
NM_001258332.2:c.493G>C
|
NP_001245261.1:p.Asp165His
|
|