ENST00000673913.2:c.1559T>G
|
ENSP00000501161.2:p.Val520Gly
|
|
ENST00000710286.1:c.1916T>G
|
ENSP00000518176.1:p.Val639Gly
|
|
ENST00000673903.1:c.1184T>G
|
ENSP00000501257.1:p.Val395Gly
|
|
ENST00000673913.1:c.299T>G
|
ENSP00000501161.1:p.Val100Gly
|
|
ENST00000302118.5:c.1559T>G
MANE Select
|
ENSP00000303208.5:p.Val520Gly
|
|
ENST00000490692.1:n.2227+894T>G
|
|
|
NM_174936.3:c.1559T>G , LRG_275t1:c.1559T>G
|
NP_777596.2:p.Val520Gly
|
|
NR_110451.1:n.1166T>G
|
|
|
XM_011541193.1:c.680T>G
|
XP_011539495.1:p.Val227Gly
|
|
NM_174936.4:c.1559T>G
MANE Select
|
NP_777596.2:p.Val520Gly
|
|
NR_110451.2:n.1166T>G
|
|
|