ENST00000357578.8:c.571C>G
MANE Select
|
ENSP00000350191.3:p.Leu191Val
|
|
ENST00000672352.1:c.334C>G
|
ENSP00000500876.1:p.Leu112Val
|
|
ENST00000672557.1:c.489C>G
|
|
|
ENST00000672652.1:c.492C>G
|
|
|
ENST00000675422.1:n.1331C>G
|
|
|
ENST00000348925.2:c.571C>G
|
ENSP00000314649.3:p.Leu191Val
|
|
ENST00000357578.7:c.571C>G
|
ENSP00000350191.3:p.Leu191Val
|
|
ENST00000491546.5:c.487C>G
|
ENSP00000417687.1:p.Leu163Val
|
|
NM_001080.3:c.571C>G
MANE Select
|
NP_001071.1:p.Leu191Val
|
|
NM_170740.1:c.571C>G
|
NP_733936.1:p.Leu191Val
|
|
NM_001368954.1:c.571C>G
|
NP_001355883.1:p.Leu191Val
|
|