ENST00000348974.5:c.807G>T
|
ENSP00000330021.7:p.Gly269=
|
|
ENST00000394236.9:c.807G>T
MANE Select
|
ENSP00000377783.3:p.Gly269=
|
|
ENST00000407433.6:c.762G>T
|
ENSP00000385794.2:p.Gly254=
|
|
ENST00000647936.1:c.807G>T
|
ENSP00000496822.1:p.Gly269=
|
|
ENST00000648381.1:n.975G>T
|
|
|
ENST00000648853.1:c.765G>T
|
ENSP00000497262.1:p.Gly255=
|
|
ENST00000649103.1:c.906G>T
|
ENSP00000497962.1:n.906G>T
|
|
ENST00000650591.1:c.903G>T
|
ENSP00000497376.1:p.Gly301=
|
|
ENST00000394236.7:c.807G>T
|
ENSP00000377783.3:p.Gly269=
|
|
ENST00000407433.5:c.414G>T
|
ENSP00000385794.1:p.Gly138=
|
|
NM_000313.3:c.807G>T , LRG_572t1:c.807G>T
|
NP_000304.2:p.Gly269=
|
|
NM_001314077.1:c.903G>T , LRG_572t2:c.903G>T
|
NP_001301006.1:p.Gly301=
|
|
NM_000313.4:c.807G>T
MANE Select
|
NP_000304.2:p.Gly269=
|
|
NM_001314077.2:c.903G>T
|
NP_001301006.1:p.Gly301=
|
|