ENST00000553591.2:c.713G>T
|
ENSP00000452421.2:p.Ser238Ile
|
|
ENST00000556293.6:n.3019G>T
|
|
|
ENST00000556754.2:n.3962G>T
|
|
|
ENST00000557229.6:n.1025G>T
|
|
|
ENST00000697613.1:c.596G>T
|
ENSP00000513359.1:p.Ser199Ile
|
|
ENST00000697614.1:c.359G>T
|
ENSP00000513360.1:p.Ser120Ile
|
|
ENST00000697615.1:n.1424G>T
|
|
|
ENST00000361505.10:c.596G>T
MANE Select
|
ENSP00000354532.6:p.Ser199Ile
|
|
ENST00000361505.9:c.596G>T
|
ENSP00000354532.5:p.Ser199Ile
|
|
ENST00000554056.5:n.904G>T
|
|
|
ENST00000556754.1:n.1813G>T
|
|
|
NM_000270.3:c.596G>T , LRG_91t1:c.596G>T
|
NP_000261.2:p.Ser199Ile
|
|
NM_000270.4:c.596G>T
MANE Select
|
NP_000261.2:p.Ser199Ile
|
|