ENST00000350721.9:c.7802G=
MANE Select
|
ENSP00000343741.4:p.Gly2601=
|
|
ENST00000513291.2:n.6511G=
|
|
|
ENST00000653893.1:n.2660G=
|
|
|
ENST00000654170.1:n.2645G=
|
|
|
ENST00000656114.1:n.2888G=
|
|
|
ENST00000656590.1:c.6729G=
|
|
|
ENST00000658083.1:n.2982G=
|
|
|
ENST00000661310.1:c.7610G=
|
ENSP00000499589.1:p.Gly2537=
|
|
ENST00000665483.1:n.5342G=
|
|
|
ENST00000666447.1:n.4305G=
|
|
|
ENST00000666943.1:n.4534G=
|
|
|
ENST00000350721.8:c.7802G=
|
ENSP00000343741.4:p.Gly2601=
|
|
ENST00000504521.5:c.391G=
|
ENSP00000422553.1:n.391G=
|
|
ENST00000513291.1:c.4866G=
|
|
|
ENST00000515810.1:c.228G=
|
ENSP00000421870.1:n.228G=
|
|
NM_001184.3:c.7802G=
|
NP_001175.2:p.Gly2601=
|
|
XM_011512924.1:c.7808G=
|
XP_011511226.1:p.Gly2603=
|
|
XM_011512925.1:c.7616G=
|
XP_011511227.1:p.Gly2539=
|
|
XR_924147.1:n.10559G=
|
|
|
XR_924148.1:n.8034G=
|
|
|
NM_001354579.1:c.7610G=
|
NP_001341508.1:p.Gly2537=
|
|
XR_001740179.2:n.8028G=
|
|
|
XR_924148.2:n.8034G=
|
|
|
NM_001184.4:c.7802G=
MANE Select
|
NP_001175.2:p.Gly2601=
|
|
NM_001354579.2:c.7610G=
|
NP_001341508.1:p.Gly2537=
|
|