ENST00000483750.6:n.798G=
|
|
|
ENST00000490627.2:n.202G=
|
|
|
ENST00000698625.1:c.765G=
|
ENSP00000513844.1:p.Gln255=
|
|
ENST00000698626.1:c.765G=
|
ENSP00000513845.1:p.Gln255=
|
|
ENST00000698635.1:c.765G=
|
ENSP00000513850.1:p.Gln255=
|
|
ENST00000376701.5:c.765G=
MANE Select
|
ENSP00000365891.4:p.Gln255=
|
|
ENST00000376701.4:c.765G=
|
ENSP00000365891.4:p.Gln255=
|
|
ENST00000465982.5:n.665G=
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|
|
ENST00000483750.5:n.791G=
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|
|
ENST00000490627.1:n.185G=
|
|
|
NM_000377.2:c.765G= , LRG_125t1:c.765G=
|
NP_000368.1:p.Gln255=
|
|
XM_011543977.1:c.765G=
|
XP_011542279.1:p.Gln255=
|
|
XM_011543977.2:c.765G=
|
XP_011542279.1:p.Gln255=
|
|
XM_017029786.1:c.765G=
|
XP_016885275.1:p.Gln255=
|
|
NM_000377.3:c.765G=
MANE Select
|
NP_000368.1:p.Gln255=
|
|