ENST00000265598.8:c.816G=
MANE Select
|
ENSP00000265598.3:p.Gly272=
|
|
ENST00000265598.7:c.816G=
|
ENSP00000265598.3:p.Gly272=
|
|
ENST00000466939.1:c.744G=
|
ENSP00000418912.1:p.Gly248=
|
|
NM_014398.3:c.816G=
|
NP_055213.2:p.Gly272=
|
|
XM_005247360.3:c.816G=
|
XP_005247417.1:p.Gly272=
|
|
XM_006713586.2:c.744G=
|
XP_006713649.1:p.Gly248=
|
|
XM_011512688.1:c.816G=
|
XP_011510990.1:p.Gly272=
|
|
XR_924123.1:n.876G=
|
|
|
XR_924124.1:n.876G=
|
|
|
XM_005247360.5:c.816G=
|
XP_005247417.1:p.Gly272=
|
|
XM_006713586.3:c.744G=
|
XP_006713649.1:p.Gly248=
|
|
XM_011512688.2:c.816G=
|
XP_011510990.1:p.Gly272=
|
|
XM_024453453.1:c.744G=
|
XP_024309221.1:p.Gly248=
|
|
NM_014398.4:c.816G=
MANE Select
|
NP_055213.2:p.Gly272=
|
|