ENST00000673913.2:c.*327A=
|
ENSP00000501161.2:n.*327A=
|
|
ENST00000710286.1:c.2344A=
|
ENSP00000518176.1:p.Thr782=
|
|
ENST00000673903.1:c.1612A=
|
ENSP00000501257.1:p.Thr538=
|
|
ENST00000673913.1:c.837A=
|
ENSP00000501161.1:n.837A=
|
|
ENST00000302118.5:c.1987A=
MANE Select
|
ENSP00000303208.5:p.Thr663=
|
|
ENST00000490692.1:n.2533A=
|
|
|
NM_174936.3:c.1987A= , LRG_275t1:c.1987A=
|
NP_777596.2:p.Thr663=
|
|
NR_110451.1:n.1594A=
|
|
|
XM_011541193.1:c.1108A=
|
XP_011539495.1:p.Thr370=
|
|
NM_174936.4:c.1987A=
MANE Select
|
NP_777596.2:p.Thr663=
|
|
NR_110451.2:n.1594A=
|
|
|