ENST00000553591.2:c.708C>A
|
ENSP00000452421.2:p.Gly236=
|
|
ENST00000556293.6:n.3014C>A
|
|
|
ENST00000556754.2:n.3957C>A
|
|
|
ENST00000557229.6:n.1020C>A
|
|
|
ENST00000697613.1:c.591C>A
|
ENSP00000513359.1:p.Gly197=
|
|
ENST00000697614.1:c.354C>A
|
ENSP00000513360.1:p.Gly118=
|
|
ENST00000697615.1:n.1419C>A
|
|
|
ENST00000361505.10:c.591C>A
MANE Select
|
ENSP00000354532.6:p.Gly197=
|
|
ENST00000361505.9:c.591C>A
|
ENSP00000354532.5:p.Gly197=
|
|
ENST00000554056.5:n.899C>A
|
|
|
ENST00000556754.1:n.1808C>A
|
|
|
NM_000270.3:c.591C>A , LRG_91t1:c.591C>A
|
NP_000261.2:p.Gly197=
|
|
NM_000270.4:c.591C>A
MANE Select
|
NP_000261.2:p.Gly197=
|
|