ENST00000587656.6:c.2732C>G
|
ENSP00000468638.2:p.Ser911Ter
|
|
ENST00000294618.12:c.2718+927C>G
MANE Select
|
ENSP00000294618.6:n.2718+927C>G
|
|
ENST00000294618.11:c.2718+927C>G
|
ENSP00000294618.6:n.2718+927C>G
|
|
ENST00000585904.1:c.335C>G
|
ENSP00000465767.1:p.Ser112Ter
|
|
ENST00000587656.5:c.492C>G
|
|
|
ENST00000590680.5:c.1061+927C>G
|
|
|
NM_020812.3:c.2718+927C>G
|
NP_065863.2:n.2718+927C>G
|
|
XM_005260000.2:c.2732C>G
|
XP_005260057.1:p.Ser911Ter
|
|
XM_005260001.2:c.2732C>G
|
XP_005260058.1:p.Ser911Ter
|
|
XM_006722804.2:c.54+763C>G
|
XP_006722867.1:n.54+763C>G
|
|
XM_011528150.1:c.2765C>G
|
XP_011526452.1:p.Ser922Ter
|
|
XM_011528151.1:c.2751+927C>G
|
XP_011526453.1:n.2751+927C>G
|
|
XM_011528152.1:c.2751+927C>G
|
XP_011526454.1:n.2751+927C>G
|
|
XM_011528153.1:c.2765C>G
|
XP_011526455.1:p.Ser922Ter
|
|
XR_936195.1:n.2826C>G
|
|
|
XR_936196.1:n.2812+927C>G
|
|
|
XR_936197.1:n.2826C>G
|
|
|
XR_936198.1:n.2812+927C>G
|
|
|
XM_006722804.3:c.54+763C>G
|
XP_006722867.1:n.54+763C>G
|
|
NM_001367830.1:c.2732C>G
|
NP_001354759.1:p.Ser911Ter
|
|
NM_020812.4:c.2718+927C>G
MANE Select
|
NP_065863.2:n.2718+927C>G
|
|