ENST00000673913.2:c.*152A=
|
ENSP00000501161.2:n.*152A=
|
|
ENST00000710286.1:c.2169A=
|
ENSP00000518176.1:p.Pro723=
|
|
ENST00000673903.1:c.1437A=
|
ENSP00000501257.1:p.Pro479=
|
|
ENST00000673913.1:c.662A=
|
ENSP00000501161.1:n.662A=
|
|
ENST00000302118.5:c.1812A=
MANE Select
|
ENSP00000303208.5:p.Pro604=
|
|
ENST00000490692.1:n.2358A=
|
|
|
NM_174936.3:c.1812A= , LRG_275t1:c.1812A=
|
NP_777596.2:p.Pro604=
|
|
NR_110451.1:n.1419A=
|
|
|
XM_011541193.1:c.933A=
|
XP_011539495.1:p.Pro311=
|
|
NM_174936.4:c.1812A=
MANE Select
|
NP_777596.2:p.Pro604=
|
|
NR_110451.2:n.1419A=
|
|
|