ENST00000673913.2:c.1621C>T
|
ENSP00000501161.2:p.Pro541Ser
|
|
ENST00000710286.1:c.1978C>T
|
ENSP00000518176.1:p.Pro660Ser
|
|
ENST00000673903.1:c.1246C>T
|
ENSP00000501257.1:p.Pro416Ser
|
|
ENST00000673913.1:c.361C>T
|
ENSP00000501161.1:p.Pro121Ser
|
|
ENST00000302118.5:c.1621C>T
MANE Select
|
ENSP00000303208.5:p.Pro541Ser
|
|
ENST00000490692.1:n.2227+956C>T
|
|
|
NM_174936.3:c.1621C>T , LRG_275t1:c.1621C>T
|
NP_777596.2:p.Pro541Ser
|
|
NR_110451.1:n.1228C>T
|
|
|
XM_011541193.1:c.742C>T
|
XP_011539495.1:p.Pro248Ser
|
|
NM_174936.4:c.1621C>T
MANE Select
|
NP_777596.2:p.Pro541Ser
|
|
NR_110451.2:n.1228C>T
|
|
|