ENST00000398603.6:c.337-206G>T
|
ENSP00000381604.1:n.337-206G>T
|
|
ENST00000398606.10:c.416G>T
MANE Select
|
ENSP00000381607.3:p.Gly139Val
|
|
ENST00000646888.1:c.*132G>T
|
ENSP00000494477.1:n.*132G>T
|
|
ENST00000398603.5:c.337-206G>T
|
ENSP00000381604.1:n.337-206G>T
|
|
ENST00000398606.7:c.416G>T
|
ENSP00000381607.3:p.Gly139Val
|
|
ENST00000467591.1:n.527G>T
|
|
|
ENST00000494593.1:n.1211G>T
|
|
|
ENST00000495996.1:c.80G>T
|
ENSP00000484686.1:p.Gly27Val
|
|
ENST00000498765.5:c.479G>T
|
|
|
NM_000852.3:c.416G>T , LRG_723t1:c.416G>T
|
NP_000843.1:p.Gly139Val
|
|
NM_000852.4:c.416G>T
MANE Select
|
NP_000843.1:p.Gly139Val
|
|