ENST00000673913.2:c.*186C>G
|
ENSP00000501161.2:n.*186C>G
|
|
ENST00000710286.1:c.2203C>G
|
ENSP00000518176.1:p.Pro735Ala
|
|
ENST00000673903.1:c.1471C>G
|
ENSP00000501257.1:p.Pro491Ala
|
|
ENST00000673913.1:c.696C>G
|
ENSP00000501161.1:n.696C>G
|
|
ENST00000302118.5:c.1846C>G
MANE Select
|
ENSP00000303208.5:p.Pro616Ala
|
|
ENST00000490692.1:n.2392C>G
|
|
|
NM_174936.3:c.1846C>G , LRG_275t1:c.1846C>G
|
NP_777596.2:p.Pro616Ala
|
|
NR_110451.1:n.1453C>G
|
|
|
XM_011541193.1:c.967C>G
|
XP_011539495.1:p.Pro323Ala
|
|
NM_174936.4:c.1846C>G
MANE Select
|
NP_777596.2:p.Pro616Ala
|
|
NR_110451.2:n.1453C>G
|
|
|