ENST00000474174.2:n.542C>T
|
|
|
ENST00000698625.1:c.1298C>T
|
ENSP00000513844.1:p.Ala433Val
|
|
ENST00000698626.1:c.1298C>T
|
ENSP00000513845.1:p.Ala433Val
|
|
ENST00000698635.1:c.1298C>T
|
ENSP00000513850.1:p.Ala433Val
|
|
ENST00000376701.5:c.1298C>T
MANE Select
|
ENSP00000365891.4:p.Ala433Val
|
|
ENST00000376701.4:c.1298C>T
|
ENSP00000365891.4:p.Ala433Val
|
|
ENST00000470107.1:n.7C>T
|
|
|
NM_000377.2:c.1298C>T , LRG_125t1:c.1298C>T
|
NP_000368.1:p.Ala433Val
|
|
XM_011543977.1:c.1142C>T
|
XP_011542279.1:p.Ala381Val
|
|
XM_011543977.2:c.1142C>T
|
XP_011542279.1:p.Ala381Val
|
|
XM_017029786.1:c.1298C>T
|
XP_016885275.1:p.Ala433Val
|
|
NM_000377.3:c.1298C>T
MANE Select
|
NP_000368.1:p.Ala433Val
|
|