ENST00000350721.9:c.6268A>G
MANE Select
|
ENSP00000343741.4:p.Met2090Val
|
|
ENST00000513291.2:n.1452A>G
|
|
|
ENST00000654170.1:n.1111A>G
|
|
|
ENST00000656590.1:c.5058A>G
|
|
|
ENST00000661310.1:c.6076A>G
|
ENSP00000499589.1:p.Met2026Val
|
|
ENST00000665483.1:n.123A>G
|
|
|
ENST00000666447.1:n.103A>G
|
|
|
ENST00000666943.1:n.1732A>G
|
|
|
ENST00000350721.8:c.6268A>G
|
ENSP00000343741.4:p.Met2090Val
|
|
NM_001184.3:c.6268A>G
|
NP_001175.2:p.Met2090Val
|
|
XM_011512924.1:c.6274A>G
|
XP_011511226.1:p.Met2092Val
|
|
XM_011512925.1:c.6082A>G
|
XP_011511227.1:p.Met2028Val
|
|
XR_924147.1:n.6363A>G
|
|
|
XR_924148.1:n.6363A>G
|
|
|
XR_924149.1:n.6242A>G
|
|
|
NM_001354579.1:c.6076A>G
|
NP_001341508.1:p.Met2026Val
|
|
XR_001740179.2:n.6357A>G
|
|
|
XR_001740180.2:n.6411A>G
|
|
|
XR_001740181.2:n.6290A>G
|
|
|
XR_001740182.1:n.6242A>G
|
|
|
XR_002959543.1:n.6467A>G
|
|
|
XR_924148.2:n.6363A>G
|
|
|
NM_001184.4:c.6268A>G
MANE Select
|
NP_001175.2:p.Met2090Val
|
|
NM_001354579.2:c.6076A>G
|
NP_001341508.1:p.Met2026Val
|
|