ENST00000673913.2:c.*137C>G
|
ENSP00000501161.2:n.*137C>G
|
|
ENST00000710286.1:c.2154C>G
|
ENSP00000518176.1:p.Ser718=
|
|
ENST00000673903.1:c.1422C>G
|
ENSP00000501257.1:p.Ser474=
|
|
ENST00000673913.1:c.647C>G
|
ENSP00000501161.1:n.647C>G
|
|
ENST00000302118.5:c.1797C>G
MANE Select
|
ENSP00000303208.5:p.Ser599=
|
|
ENST00000490692.1:n.2343C>G
|
|
|
NM_174936.3:c.1797C>G , LRG_275t1:c.1797C>G
|
NP_777596.2:p.Ser599=
|
|
NR_110451.1:n.1404C>G
|
|
|
XM_011541193.1:c.918C>G
|
XP_011539495.1:p.Ser306=
|
|
NM_174936.4:c.1797C>G
MANE Select
|
NP_777596.2:p.Ser599=
|
|
NR_110451.2:n.1404C>G
|
|
|