NM_005224.3:c.1653C>T
MANE Select
|
NP_005215.1:p.Gly551=
|
ENST00000263620.8:c.1653C>T
MANE Select
|
ENSP00000263620.2:p.Gly551=
|
NM_005224.2:c.1653C>T
|
NP_005215.1:p.Gly551=
|
ENST00000263620.7:c.1653C>T
|
ENSP00000263620.2:p.Gly551=
|
ENST00000587532.5:c.897C>T
|
ENSP00000464969.3:p.Gly299=
|
XM_005259513.3:c.1653C>T
|
XP_005259570.1:p.Gly551=
|
XM_005259513.5:c.1653C>T
|
XP_005259570.1:p.Gly551=
|
XM_005259514.3:c.1653C>T
|
XP_005259571.1:p.Gly551=
|
XM_005259514.4:c.1653C>T
|
XP_005259571.1:p.Gly551=
|
XM_017026445.1:c.1653C>T
|
XP_016881934.1:p.Gly551=
|
XM_017026446.1:c.900C>T
|
XP_016881935.1:p.Gly300=
|
XM_024451407.1:c.900C>T
|
XP_024307175.1:p.Gly300=
|