ENST00000623535.2:c.2655G=
MANE Select
|
ENSP00000485244.1:p.Gly885=
|
|
ENST00000674046.1:c.2778G=
|
ENSP00000501174.1:p.Gly926=
|
|
ENST00000379989.6:c.2655G=
|
ENSP00000369325.3:p.Gly885=
|
|
ENST00000379996.7:c.2655G=
|
ENSP00000369332.3:p.Gly885=
|
|
ENST00000623535.1:c.2655G=
|
ENSP00000485244.1:p.Gly885=
|
|
NM_001037343.1:c.2655G=
|
NP_001032420.1:p.Gly885=
|
|
NM_003159.2:c.2655G=
|
NP_003150.1:p.Gly885=
|
|
XM_011545569.1:c.2727G=
|
XP_011543871.1:p.Gly909=
|
|
XM_011545570.1:c.2646G=
|
XP_011543872.1:p.Gly882=
|
|
XR_950484.1:n.3030G=
|
|
|
NM_001323289.1:c.2655G=
|
NP_001310218.1:p.Gly885=
|
|
NM_001323289.2:c.2655G=
MANE Select
|
NP_001310218.1:p.Gly885=
|
|
NM_001037343.2:c.2655G=
|
NP_001032420.1:p.Gly885=
|
|
NM_003159.3:c.2655G=
|
NP_003150.1:p.Gly885=
|
|