ENST00000350721.9:c.6257C>G
MANE Select
|
ENSP00000343741.4:p.Ser2086Ter
|
|
ENST00000513291.2:n.1441C>G
|
|
|
ENST00000654170.1:n.1100C>G
|
|
|
ENST00000656590.1:c.5047C>G
|
|
|
ENST00000661310.1:c.6065C>G
|
ENSP00000499589.1:p.Ser2022Ter
|
|
ENST00000665483.1:n.112C>G
|
|
|
ENST00000666447.1:n.92C>G
|
|
|
ENST00000666943.1:n.1721C>G
|
|
|
ENST00000350721.8:c.6257C>G
|
ENSP00000343741.4:p.Ser2086Ter
|
|
NM_001184.3:c.6257C>G
|
NP_001175.2:p.Ser2086Ter
|
|
XM_011512924.1:c.6263C>G
|
XP_011511226.1:p.Ser2088Ter
|
|
XM_011512925.1:c.6071C>G
|
XP_011511227.1:p.Ser2024Ter
|
|
XR_924147.1:n.6352C>G
|
|
|
XR_924148.1:n.6352C>G
|
|
|
XR_924149.1:n.6231C>G
|
|
|
NM_001354579.1:c.6065C>G
|
NP_001341508.1:p.Ser2022Ter
|
|
XR_001740179.2:n.6346C>G
|
|
|
XR_001740180.2:n.6400C>G
|
|
|
XR_001740181.2:n.6279C>G
|
|
|
XR_001740182.1:n.6231C>G
|
|
|
XR_002959543.1:n.6456C>G
|
|
|
XR_924148.2:n.6352C>G
|
|
|
NM_001184.4:c.6257C>G
MANE Select
|
NP_001175.2:p.Ser2086Ter
|
|
NM_001354579.2:c.6065C>G
|
NP_001341508.1:p.Ser2022Ter
|
|