ENST00000673913.2:c.1618C>T
|
ENSP00000501161.2:p.Pro540Ser
|
|
ENST00000710286.1:c.1975C>T
|
ENSP00000518176.1:p.Pro659Ser
|
|
ENST00000673903.1:c.1243C>T
|
ENSP00000501257.1:p.Pro415Ser
|
|
ENST00000673913.1:c.358C>T
|
ENSP00000501161.1:p.Pro120Ser
|
|
ENST00000302118.5:c.1618C>T
MANE Select
|
ENSP00000303208.5:p.Pro540Ser
|
|
ENST00000490692.1:n.2227+953C>T
|
|
|
NM_174936.3:c.1618C>T , LRG_275t1:c.1618C>T
|
NP_777596.2:p.Pro540Ser
|
|
NR_110451.1:n.1225C>T
|
|
|
XM_011541193.1:c.739C>T
|
XP_011539495.1:p.Pro247Ser
|
|
NM_174936.4:c.1618C>T
MANE Select
|
NP_777596.2:p.Pro540Ser
|
|
NR_110451.2:n.1225C>T
|
|
|