NM_000203.5:c.1225G=
MANE Select
|
NP_000194.2:p.Gly409=
|
ENST00000514224.2:c.1225G=
MANE Select
|
ENSP00000425081.2:p.Gly409=
|
NM_000203.4:c.1225G=
|
NP_000194.2:p.Gly409=
|
NM_001363576.1:c.829G=
|
NP_001350505.1:p.Gly277=
|
NR_110313.1:n.1313G=
|
|
ENST00000247933.8:c.1225G=
|
ENSP00000247933.4:p.Gly409=
|
ENST00000247933.9:c.1225G=
|
ENSP00000247933.4:p.Gly409=
|
ENST00000502829.1:n.27G=
|
|
ENST00000514224.1:c.829G=
|
ENSP00000425081.1:p.Gly277=
|
ENST00000514698.5:n.1332G=
|
|
ENST00000652070.1:n.1281G=
|
|
XM_006713882.2:c.829G=
|
XP_006713945.1:p.Gly277=
|
XM_011513459.1:c.1291G=
|
XP_011511761.1:p.Gly431=
|
XM_011513460.1:c.1084G=
|
XP_011511762.1:p.Gly362=
|
XM_011513461.1:c.1018G=
|
XP_011511763.1:p.Gly340=
|
XM_011513461.2:c.1018G=
|
XP_011511763.1:p.Gly340=
|
XM_011513462.1:c.937G=
|
XP_011511764.1:p.Gly313=
|
XM_011513463.1:c.937G=
|
XP_011511765.1:p.Gly313=
|
XM_017008163.1:c.265G=
|
XP_016863652.1:p.Gly89=
|
XR_924947.1:n.1294G=
|
|