ENST00000366641.4:c.1111C>T
MANE Select
|
ENSP00000355601.3:p.Arg371Cys
|
|
ENST00000476717.2:n.388C>T
|
|
|
ENST00000653198.1:n.653C>T
|
|
|
ENST00000653908.1:c.151-2963C>T
|
ENSP00000499669.1:n.151-2963C>T
|
|
ENST00000654803.1:c.333C>T
|
|
|
ENST00000658954.1:c.485C>T
|
|
|
ENST00000662216.1:c.250C>T
|
ENSP00000499467.1:p.Arg84Cys
|
|
ENST00000663780.1:n.211C>T
|
|
|
ENST00000667629.1:c.316-2963C>T
|
ENSP00000499629.1:n.316-2963C>T
|
|
ENST00000670301.1:c.230-4124C>T
|
|
|
ENST00000366641.3:c.1111C>T
|
ENSP00000355601.3:p.Arg371Cys
|
|
ENST00000476717.1:n.388C>T
|
|
|
NM_022051.2:c.1111C>T
|
NP_071334.1:p.Arg371Cys
|
|
XM_005273166.3:c.1111C>T
|
XP_005273223.1:p.Arg371Cys
|
|
XM_005273167.3:c.1012-2963C>T
|
XP_005273224.1:n.1012-2963C>T
|
|
XM_005273166.5:c.1111C>T
|
XP_005273223.1:p.Arg371Cys
|
|
XM_005273167.5:c.1012-2963C>T
|
XP_005273224.1:n.1012-2963C>T
|
|
XM_024447734.1:c.1012-2963C>T
|
XP_024303502.1:n.1012-2963C>T
|
|
NM_001377260.1:c.1111C>T
|
NP_001364189.1:p.Arg371Cys
|
|
NM_001377261.1:c.1012-2963C>T
|
NP_001364190.1:n.1012-2963C>T
|
|
NM_022051.3:c.1111C>T
MANE Select
|
NP_071334.1:p.Arg371Cys
|
|