ENST00000691183.1:c.*408+2T>C
|
ENSP00000509954.1:n.*408+2T>C
|
|
ENST00000378842.8:c.820+2T>C
MANE Select
|
ENSP00000368119.4:n.820+2T>C
|
|
ENST00000378842.7:c.820+2T>C
|
ENSP00000368119.3:n.820+2T>C
|
|
ENST00000450095.6:c.493+2T>C
|
ENSP00000401956.2:n.493+2T>C
|
|
ENST00000489643.6:n.900+2T>C
|
|
|
ENST00000554085.5:c.*564+2T>C
|
ENSP00000450419.1:n.*564+2T>C
|
|
ENST00000554550.5:c.*440+2T>C
|
ENSP00000451435.1:n.*440+2T>C
|
|
ENST00000554638.5:n.1292+2T>C
|
|
|
ENST00000555020.5:n.1281+2T>C
|
|
|
ENST00000555086.5:n.826T>C
|
|
|
ENST00000555754.1:n.167T>C
|
|
|
ENST00000556278.1:c.432+440T>C
|
ENSP00000451792.1:n.432+440T>C
|
|
ENST00000557706.5:n.1384T>C
|
|
|
NM_000155.3:c.820+2T>C
|
NP_000146.2:n.820+2T>C
|
|
NM_001258332.1:c.493+2T>C
|
NP_001245261.1:n.493+2T>C
|
|
NM_000155.4:c.820+2T>C
MANE Select
|
NP_000146.2:n.820+2T>C
|
|
NM_001258332.2:c.493+2T>C
|
NP_001245261.1:n.493+2T>C
|
|