ENST00000357578.8:c.1265C>G
MANE Select
|
ENSP00000350191.3:p.Pro422Arg
|
|
ENST00000479394.2:n.380C>G
|
|
|
ENST00000672352.1:c.884C>G
|
ENSP00000500876.1:p.Pro295Arg
|
|
ENST00000672652.1:c.1228C>G
|
|
|
ENST00000348925.2:c.1304C>G
|
ENSP00000314649.3:p.Pro435Arg
|
|
ENST00000357578.7:c.1265C>G
|
ENSP00000350191.3:p.Pro422Arg
|
|
ENST00000479394.1:n.380C>G
|
|
|
ENST00000491546.5:c.1181C>G
|
ENSP00000417687.1:p.Pro394Arg
|
|
NM_001080.3:c.1265C>G
MANE Select
|
NP_001071.1:p.Pro422Arg
|
|
NM_170740.1:c.1304C>G
|
NP_733936.1:p.Pro435Arg
|
|
NM_001368954.1:c.1121C>G
|
NP_001355883.1:p.Pro374Arg
|
|