ENST00000262494.13:c.491G=
|
ENSP00000262494.7:p.Gly164=
|
|
ENST00000262493.12:c.491G=
MANE Select
|
ENSP00000262493.6:p.Gly164=
|
|
ENST00000262494.12:c.491G=
|
ENSP00000262494.7:p.Gly164=
|
|
ENST00000562316.6:c.158G=
|
ENSP00000457238.2:p.Gly53=
|
|
ENST00000638185.1:n.706G=
|
|
|
ENST00000638210.1:n.791G=
|
|
|
ENST00000638705.1:c.491G=
|
ENSP00000491223.1:p.Gly164=
|
|
ENST00000638836.1:n.401G=
|
|
|
ENST00000639055.1:n.1212G=
|
|
|
ENST00000639251.1:n.392G=
|
|
|
ENST00000639268.1:c.229-1976G=
|
|
|
ENST00000639341.1:c.16G=
|
|
|
ENST00000639770.1:c.529G=
|
ENSP00000491999.1:n.529G=
|
|
ENST00000640390.1:n.421G=
|
|
|
ENST00000640893.1:c.330G=
|
ENSP00000492677.1:p.Trp110=
|
|
ENST00000262493.10:c.491G=
|
ENSP00000262493.6:p.Gly164=
|
|
ENST00000262494.11:c.491G=
|
ENSP00000262494.7:p.Gly164=
|
|
ENST00000562316.5:c.230G=
|
ENSP00000457238.1:p.Gly77=
|
|
ENST00000563440.1:c.230G=
|
ENSP00000455774.1:p.Gly77=
|
|
ENST00000565363.5:c.365G=
|
ENSP00000454728.1:p.Gly122=
|
|
NM_020988.2:c.491G=
|
NP_066268.1:p.Gly164=
|
|
NM_138736.2:c.491G=
|
NP_620073.2:p.Gly164=
|
|
XM_011523003.1:c.365G=
|
XP_011521305.1:p.Gly122=
|
|
XM_011523003.3:c.365G=
|
XP_011521305.1:p.Gly122=
|
|
NM_020988.3:c.491G=
MANE Select
|
NP_066268.1:p.Gly164=
|
|
NM_138736.3:c.491G=
|
NP_620073.2:p.Gly164=
|
|