ENST00000350721.9:c.6235G>T
MANE Select
|
ENSP00000343741.4:p.Gly2079Ter
|
|
ENST00000513291.2:n.1419G>T
|
|
|
ENST00000654170.1:n.1078G>T
|
|
|
ENST00000656590.1:c.5025G>T
|
|
|
ENST00000661310.1:c.6043G>T
|
ENSP00000499589.1:p.Gly2015Ter
|
|
ENST00000665483.1:n.90G>T
|
|
|
ENST00000666447.1:n.70G>T
|
|
|
ENST00000666943.1:n.1699G>T
|
|
|
ENST00000350721.8:c.6235G>T
|
ENSP00000343741.4:p.Gly2079Ter
|
|
NM_001184.3:c.6235G>T
|
NP_001175.2:p.Gly2079Ter
|
|
XM_011512924.1:c.6241G>T
|
XP_011511226.1:p.Gly2081Ter
|
|
XM_011512925.1:c.6049G>T
|
XP_011511227.1:p.Gly2017Ter
|
|
XR_924147.1:n.6330G>T
|
|
|
XR_924148.1:n.6330G>T
|
|
|
XR_924149.1:n.6209G>T
|
|
|
NM_001354579.1:c.6043G>T
|
NP_001341508.1:p.Gly2015Ter
|
|
XR_001740179.2:n.6324G>T
|
|
|
XR_001740180.2:n.6378G>T
|
|
|
XR_001740181.2:n.6257G>T
|
|
|
XR_001740182.1:n.6209G>T
|
|
|
XR_002959543.1:n.6434G>T
|
|
|
XR_924148.2:n.6330G>T
|
|
|
NM_001184.4:c.6235G>T
MANE Select
|
NP_001175.2:p.Gly2079Ter
|
|
NM_001354579.2:c.6043G>T
|
NP_001341508.1:p.Gly2015Ter
|
|