ENST00000360228.11:c.5358T>C
MANE Select
|
ENSP00000353362.5:p.Ala1786=
|
|
ENST00000573710.7:c.5364T>C
|
ENSP00000460092.3:p.Ala1788=
|
|
ENST00000573891.6:c.777T>C
|
|
|
ENST00000574822.6:n.582T>C
|
|
|
ENST00000585802.6:c.519T>C
|
ENSP00000465598.2:p.Ala173=
|
|
ENST00000635727.1:c.5361T>C
|
ENSP00000490001.1:p.Ala1787=
|
|
ENST00000635742.1:n.1347T>C
|
|
|
ENST00000635895.1:c.5361T>C
|
ENSP00000490323.1:p.Ala1787=
|
|
ENST00000636012.1:c.5361T>C
|
ENSP00000490223.1:p.Ala1787=
|
|
ENST00000636389.1:c.5361T>C
|
ENSP00000489992.1:p.Ala1787=
|
|
ENST00000636473.1:c.453T>C
|
ENSP00000490173.1:p.Ala151=
|
|
ENST00000636549.1:c.5367T>C
|
ENSP00000490578.1:p.Ala1789=
|
|
ENST00000637276.1:c.5361T>C
|
ENSP00000489777.1:p.Ala1787=
|
|
ENST00000637432.1:c.5376T>C
|
ENSP00000490617.1:p.Ala1792=
|
|
ENST00000637736.1:c.5220T>C
|
ENSP00000489861.1:p.Ala1740=
|
|
ENST00000637769.1:c.5361T>C
|
ENSP00000489778.1:p.Ala1787=
|
|
ENST00000637777.1:c.552T>C
|
|
|
ENST00000637809.1:n.751T>C
|
|
|
ENST00000637819.1:c.762T>C
|
ENSP00000490686.1:p.Ala254=
|
|
ENST00000637832.1:n.352T>C
|
|
|
ENST00000637927.1:c.5364T>C
|
ENSP00000489715.1:p.Ala1788=
|
|
ENST00000638009.2:c.5361T>C
|
ENSP00000489913.1:p.Ala1787=
|
|
ENST00000638029.1:c.5376T>C
|
ENSP00000489829.1:p.Ala1792=
|
|
ENST00000664864.1:c.5562T>C
|
ENSP00000499449.1:p.Ala1854=
|
|
ENST00000360228.9:c.5358T>C
|
ENSP00000353362.5:p.Ala1786=
|
|
ENST00000573710.6:c.5361T>C
|
ENSP00000460092.2:p.Ala1787=
|
|
ENST00000573891.5:c.777T>C
|
|
|
ENST00000574822.5:n.582T>C
|
|
|
ENST00000585802.5:c.1416T>C
|
ENSP00000465598.1:p.Ala472=
|
|
ENST00000587525.5:c.819T>C
|
ENSP00000467729.1:p.Ala273=
|
|
ENST00000614285.4:c.5376T>C
|
ENSP00000479983.1:p.Ala1792=
|
|
NM_000068.3:c.5376T>C
|
NP_000059.3:p.Ala1792=
|
|
NM_001127221.1:c.5361T>C , LRG_7t1:c.5361T>C
|
NP_001120693.1:p.Ala1787=
|
|
NM_001127222.1:c.5358T>C
|
NP_001120694.1:p.Ala1786=
|
|
NM_001174080.1:c.5367T>C
|
NP_001167551.1:p.Ala1789=
|
|
NM_023035.2:c.5376T>C
|
NP_075461.2:p.Ala1792=
|
|
NM_000068.4:c.5376T>C
|
NP_000059.3:p.Ala1792=
|
|
NM_001127222.2:c.5358T>C
MANE Select
|
NP_001120694.1:p.Ala1786=
|
|
NM_001174080.2:c.5367T>C
|
NP_001167551.1:p.Ala1789=
|
|
NM_023035.3:c.5376T>C
|
NP_075461.2:p.Ala1792=
|
|
NM_001127221.2:c.5361T>C
|
NP_001120693.1:p.Ala1787=
|
|