ENST00000474174.2:n.568A>G
|
|
|
ENST00000698625.1:c.1324A>G
|
ENSP00000513844.1:p.Ile442Val
|
|
ENST00000698626.1:c.1324A>G
|
ENSP00000513845.1:p.Ile442Val
|
|
ENST00000698635.1:c.1324A>G
|
ENSP00000513850.1:p.Ile442Val
|
|
ENST00000376701.5:c.1324A>G
MANE Select
|
ENSP00000365891.4:p.Ile442Val
|
|
ENST00000376701.4:c.1324A>G
|
ENSP00000365891.4:p.Ile442Val
|
|
ENST00000470107.1:n.33A>G
|
|
|
NM_000377.2:c.1324A>G , LRG_125t1:c.1324A>G
|
NP_000368.1:p.Ile442Val
|
|
XM_011543977.1:c.1168A>G
|
XP_011542279.1:p.Ile390Val
|
|
XM_011543977.2:c.1168A>G
|
XP_011542279.1:p.Ile390Val
|
|
XM_017029786.1:c.1324A>G
|
XP_016885275.1:p.Ile442Val
|
|
NM_000377.3:c.1324A>G
MANE Select
|
NP_000368.1:p.Ile442Val
|
|