ENST00000360228.11:c.3992G>C
MANE Select
|
ENSP00000353362.5:p.Gly1331Ala
|
|
ENST00000573710.7:c.3998G>C
|
ENSP00000460092.3:p.Gly1333Ala
|
|
ENST00000635727.1:c.3995G>C
|
ENSP00000490001.1:p.Gly1332Ala
|
|
ENST00000635895.1:c.3995G>C
|
ENSP00000490323.1:p.Gly1332Ala
|
|
ENST00000635917.1:n.484G>C
|
|
|
ENST00000636012.1:c.3995G>C
|
ENSP00000490223.1:p.Gly1332Ala
|
|
ENST00000636389.1:c.3995G>C
|
ENSP00000489992.1:p.Gly1332Ala
|
|
ENST00000636549.1:c.3995G>C
|
ENSP00000490578.1:p.Gly1332Ala
|
|
ENST00000636816.1:n.680G>C
|
|
|
ENST00000637004.1:n.458G>C
|
|
|
ENST00000637276.1:c.3995G>C
|
ENSP00000489777.1:p.Gly1332Ala
|
|
ENST00000637432.1:c.4004G>C
|
ENSP00000490617.1:p.Gly1335Ala
|
|
ENST00000637692.1:n.314G>C
|
|
|
ENST00000637736.1:c.3854G>C
|
ENSP00000489861.1:p.Gly1285Ala
|
|
ENST00000637769.1:c.3995G>C
|
ENSP00000489778.1:p.Gly1332Ala
|
|
ENST00000637927.1:c.3998G>C
|
ENSP00000489715.1:p.Gly1333Ala
|
|
ENST00000638009.2:c.3995G>C
|
ENSP00000489913.1:p.Gly1332Ala
|
|
ENST00000638029.1:c.4004G>C
|
ENSP00000489829.1:p.Gly1335Ala
|
|
ENST00000664864.1:c.4190G>C
|
ENSP00000499449.1:p.Gly1397Ala
|
|
ENST00000360228.9:c.3992G>C
|
ENSP00000353362.5:p.Gly1331Ala
|
|
ENST00000573710.6:c.3995G>C
|
ENSP00000460092.2:p.Gly1332Ala
|
|
ENST00000585802.5:c.50G>C
|
ENSP00000465598.1:p.Gly17Ala
|
|
ENST00000590205.1:n.71G>C
|
|
|
ENST00000614285.4:c.4004G>C
|
ENSP00000479983.1:p.Gly1335Ala
|
|
NM_000068.3:c.4004G>C
|
NP_000059.3:p.Gly1335Ala
|
|
NM_001127221.1:c.3995G>C , LRG_7t1:c.3995G>C
|
NP_001120693.1:p.Gly1332Ala
|
|
NM_001127222.1:c.3992G>C
|
NP_001120694.1:p.Gly1331Ala
|
|
NM_001174080.1:c.3995G>C
|
NP_001167551.1:p.Gly1332Ala
|
|
NM_023035.2:c.4004G>C
|
NP_075461.2:p.Gly1335Ala
|
|
NM_000068.4:c.4004G>C
|
NP_000059.3:p.Gly1335Ala
|
|
NM_001127222.2:c.3992G>C
MANE Select
|
NP_001120694.1:p.Gly1331Ala
|
|
NM_001174080.2:c.3995G>C
|
NP_001167551.1:p.Gly1332Ala
|
|
NM_023035.3:c.4004G>C
|
NP_075461.2:p.Gly1335Ala
|
|
NM_001127221.2:c.3995G>C
|
NP_001120693.1:p.Gly1332Ala
|
|