ENST00000553591.2:c.227G>T
|
ENSP00000452421.2:p.Gly76Val
|
|
ENST00000556293.6:n.229G>T
|
|
|
ENST00000556754.2:n.1172G>T
|
|
|
ENST00000557229.6:n.229G>T
|
|
|
ENST00000697613.1:c.110G>T
|
ENSP00000513359.1:p.Gly37Val
|
|
ENST00000697614.1:c.-128G>T
|
ENSP00000513360.1:n.-128G>T
|
|
ENST00000697615.1:n.628G>T
|
|
|
ENST00000361505.10:c.110G>T
MANE Select
|
ENSP00000354532.6:p.Gly37Val
|
|
ENST00000361505.9:c.110G>T
|
ENSP00000354532.5:p.Gly37Val
|
|
ENST00000553418.5:c.110G>T
|
ENSP00000450663.1:p.Gly37Val
|
|
ENST00000553591.1:c.227G>T
|
ENSP00000452421.1:p.Gly76Val
|
|
ENST00000554056.5:n.221G>T
|
|
|
ENST00000554065.1:c.-128G>T
|
ENSP00000451108.1:n.-128G>T
|
|
ENST00000556293.5:n.229G>T
|
|
|
ENST00000557229.5:n.229G>T
|
|
|
NM_000270.3:c.110G>T , LRG_91t1:c.110G>T
|
NP_000261.2:p.Gly37Val
|
|
NM_000270.4:c.110G>T
MANE Select
|
NP_000261.2:p.Gly37Val
|
|