ENST00000673913.2:c.*257T>A
|
ENSP00000501161.2:n.*257T>A
|
|
ENST00000710286.1:c.2274T>A
|
ENSP00000518176.1:p.Pro758=
|
|
ENST00000673903.1:c.1542T>A
|
ENSP00000501257.1:p.Pro514=
|
|
ENST00000673913.1:c.767T>A
|
ENSP00000501161.1:n.767T>A
|
|
ENST00000302118.5:c.1917T>A
MANE Select
|
ENSP00000303208.5:p.Pro639=
|
|
ENST00000490692.1:n.2463T>A
|
|
|
NM_174936.3:c.1917T>A , LRG_275t1:c.1917T>A
|
NP_777596.2:p.Pro639=
|
|
NR_110451.1:n.1524T>A
|
|
|
XM_011541193.1:c.1038T>A
|
XP_011539495.1:p.Pro346=
|
|
NM_174936.4:c.1917T>A
MANE Select
|
NP_777596.2:p.Pro639=
|
|
NR_110451.2:n.1524T>A
|
|
|