ENST00000483750.6:n.795C>G
|
|
|
ENST00000490627.2:n.199C>G
|
|
|
ENST00000698625.1:c.762C>G
|
ENSP00000513844.1:p.Pro254=
|
|
ENST00000698626.1:c.762C>G
|
ENSP00000513845.1:p.Pro254=
|
|
ENST00000698635.1:c.762C>G
|
ENSP00000513850.1:p.Pro254=
|
|
ENST00000376701.5:c.762C>G
MANE Select
|
ENSP00000365891.4:p.Pro254=
|
|
ENST00000376701.4:c.762C>G
|
ENSP00000365891.4:p.Pro254=
|
|
ENST00000465982.5:n.662C>G
|
|
|
ENST00000483750.5:n.788C>G
|
|
|
ENST00000490627.1:n.182C>G
|
|
|
NM_000377.2:c.762C>G , LRG_125t1:c.762C>G
|
NP_000368.1:p.Pro254=
|
|
XM_011543977.1:c.762C>G
|
XP_011542279.1:p.Pro254=
|
|
XM_011543977.2:c.762C>G
|
XP_011542279.1:p.Pro254=
|
|
XM_017029786.1:c.762C>G
|
XP_016885275.1:p.Pro254=
|
|
NM_000377.3:c.762C>G
MANE Select
|
NP_000368.1:p.Pro254=
|
|