ENST00000673913.2:c.*129C>A
|
ENSP00000501161.2:n.*129C>A
|
|
ENST00000710286.1:c.2146C>A
|
ENSP00000518176.1:p.His716Asn
|
|
ENST00000673903.1:c.1414C>A
|
ENSP00000501257.1:p.His472Asn
|
|
ENST00000673913.1:c.639C>A
|
ENSP00000501161.1:n.639C>A
|
|
ENST00000302118.5:c.1789C>A
MANE Select
|
ENSP00000303208.5:p.His597Asn
|
|
ENST00000490692.1:n.2335C>A
|
|
|
NM_174936.3:c.1789C>A , LRG_275t1:c.1789C>A
|
NP_777596.2:p.His597Asn
|
|
NR_110451.1:n.1396C>A
|
|
|
XM_011541193.1:c.910C>A
|
XP_011539495.1:p.His304Asn
|
|
NM_174936.4:c.1789C>A
MANE Select
|
NP_777596.2:p.His597Asn
|
|
NR_110451.2:n.1396C>A
|
|
|