ENST00000261769.10:c.1907C>G
MANE Select
|
ENSP00000261769.4:p.Ala636Gly
|
|
ENST00000261769.9:c.1907C>G
|
ENSP00000261769.4:p.Ala636Gly
|
|
ENST00000422392.6:c.1724C>G
|
ENSP00000414946.2:p.Ala575Gly
|
|
ENST00000562836.5:n.1978C>G
|
|
|
ENST00000566510.5:c.*573C>G
|
ENSP00000458139.1:n.*573C>G
|
|
ENST00000566612.5:c.*147C>G
|
ENSP00000454782.1:n.*147C>G
|
|
ENST00000611625.4:c.1970C>G
|
ENSP00000481063.1:p.Ala657Gly
|
|
ENST00000612417.4:c.1830+77C>G
|
ENSP00000478360.1:n.1830+77C>G
|
|
ENST00000621016.4:c.1865+42C>G
|
ENSP00000480664.1:n.1865+42C>G
|
|
NM_004360.3:c.1907C>G , LRG_301t1:c.1907C>G
|
NP_004351.1:p.Ala636Gly
|
|
XM_011523488.1:c.1172C>G
|
XP_011521790.1:p.Ala391Gly
|
|
XM_011523489.1:c.1172C>G
|
XP_011521791.1:p.Ala391Gly
|
|
NM_001317184.1:c.1724C>G
|
NP_001304113.1:p.Ala575Gly
|
|
NM_001317185.1:c.359C>G
|
NP_001304114.1:p.Ala120Gly
|
|
NM_001317186.1:c.-59C>G
|
NP_001304115.1:n.-59C>G
|
|
NM_004360.4:c.1907C>G
|
NP_004351.1:p.Ala636Gly
|
|
NM_004360.5:c.1907C>G
MANE Select
|
NP_004351.1:p.Ala636Gly
|
|
NM_001317184.2:c.1724C>G
|
NP_001304113.1:p.Ala575Gly
|
|
NM_001317185.2:c.359C>G
|
NP_001304114.1:p.Ala120Gly
|
|
NM_001317186.2:c.-59C>G
|
NP_001304115.1:n.-59C>G
|
|