ENST00000265598.8:c.825_826delinsCA
MANE Select
|
ENSP00000265598.3:p.Gly275=
|
|
ENST00000265598.7:c.825_826delinsCA
|
ENSP00000265598.3:p.Gly275=
|
|
ENST00000466939.1:c.753_754delinsCA
|
ENSP00000418912.1:p.Gly251=
|
|
NM_014398.3:c.825_826delinsCA
|
NP_055213.2:p.Gly275=
|
|
XM_005247360.3:c.825_826delinsCA
|
XP_005247417.1:p.Gly275=
|
|
XM_006713586.2:c.753_754delinsCA
|
XP_006713649.1:p.Gly251=
|
|
XM_011512688.1:c.825_826delinsCA
|
XP_011510990.1:p.Gly275=
|
|
XR_924123.1:n.885_886delinsCA
|
|
|
XR_924124.1:n.885_886delinsCA
|
|
|
XM_005247360.5:c.825_826delinsCA
|
XP_005247417.1:p.Gly275=
|
|
XM_006713586.3:c.753_754delinsCA
|
XP_006713649.1:p.Gly251=
|
|
XM_011512688.2:c.825_826delinsCA
|
XP_011510990.1:p.Gly275=
|
|
XM_024453453.1:c.753_754delinsCA
|
XP_024309221.1:p.Gly251=
|
|
NM_014398.4:c.825_826delinsCA
MANE Select
|
NP_055213.2:p.Gly275=
|
|