ENST00000350721.9:c.6258A>G
MANE Select
|
ENSP00000343741.4:p.Ser2086=
|
|
ENST00000513291.2:n.1442A>G
|
|
|
ENST00000654170.1:n.1101A>G
|
|
|
ENST00000656590.1:c.5048A>G
|
|
|
ENST00000661310.1:c.6066A>G
|
ENSP00000499589.1:p.Ser2022=
|
|
ENST00000665483.1:n.113A>G
|
|
|
ENST00000666447.1:n.93A>G
|
|
|
ENST00000666943.1:n.1722A>G
|
|
|
ENST00000350721.8:c.6258A>G
|
ENSP00000343741.4:p.Ser2086=
|
|
NM_001184.3:c.6258A>G
|
NP_001175.2:p.Ser2086=
|
|
XM_011512924.1:c.6264A>G
|
XP_011511226.1:p.Ser2088=
|
|
XM_011512925.1:c.6072A>G
|
XP_011511227.1:p.Ser2024=
|
|
XR_924147.1:n.6353A>G
|
|
|
XR_924148.1:n.6353A>G
|
|
|
XR_924149.1:n.6232A>G
|
|
|
NM_001354579.1:c.6066A>G
|
NP_001341508.1:p.Ser2022=
|
|
XR_001740179.2:n.6347A>G
|
|
|
XR_001740180.2:n.6401A>G
|
|
|
XR_001740181.2:n.6280A>G
|
|
|
XR_001740182.1:n.6232A>G
|
|
|
XR_002959543.1:n.6457A>G
|
|
|
XR_924148.2:n.6353A>G
|
|
|
NM_001184.4:c.6258A>G
MANE Select
|
NP_001175.2:p.Ser2086=
|
|
NM_001354579.2:c.6066A>G
|
NP_001341508.1:p.Ser2022=
|
|