ENST00000601549.2:n.481C>G
|
|
|
ENST00000648053.1:n.291C>G
|
|
|
ENST00000648319.1:c.859C>G
MANE Select
|
ENSP00000496939.1:p.Arg287Gly
|
|
ENST00000262888.7:c.859C>G
|
ENSP00000262888.3:p.Arg287Gly
|
|
ENST00000598836.1:c.38C>G
|
|
|
ENST00000599720.5:c.*129C>G
|
ENSP00000472513.1:n.*129C>G
|
|
ENST00000600408.1:c.148C>G
|
ENSP00000472510.1:p.Arg50Gly
|
|
ENST00000601549.1:n.168C>G
|
|
|
ENST00000615047.4:c.463C>G
|
ENSP00000485014.1:p.Arg155Gly
|
|
NM_002250.2:c.859C>G
|
NP_002241.1:p.Arg287Gly
|
|
XM_005258882.2:c.763C>G
|
XP_005258939.1:p.Arg255Gly
|
|
XM_005258883.2:c.670C>G
|
XP_005258940.1:p.Arg224Gly
|
|
XR_935823.1:n.2105C>G
|
|
|
XR_002958313.1:n.2251C>G
|
|
|
NM_002250.3:c.859C>G
MANE Select
|
NP_002241.1:p.Arg287Gly
|
|