ENST00000350721.9:c.6290A>C
MANE Select
|
ENSP00000343741.4:p.Tyr2097Ser
|
|
ENST00000513291.2:n.1474A>C
|
|
|
ENST00000654170.1:n.1133A>C
|
|
|
ENST00000656590.1:c.5080A>C
|
|
|
ENST00000661310.1:c.6098A>C
|
ENSP00000499589.1:p.Tyr2033Ser
|
|
ENST00000665483.1:n.145A>C
|
|
|
ENST00000666447.1:n.125A>C
|
|
|
ENST00000666943.1:n.1754A>C
|
|
|
ENST00000350721.8:c.6290A>C
|
ENSP00000343741.4:p.Tyr2097Ser
|
|
NM_001184.3:c.6290A>C
|
NP_001175.2:p.Tyr2097Ser
|
|
XM_011512924.1:c.6296A>C
|
XP_011511226.1:p.Tyr2099Ser
|
|
XM_011512925.1:c.6104A>C
|
XP_011511227.1:p.Tyr2035Ser
|
|
XR_924147.1:n.6385A>C
|
|
|
XR_924148.1:n.6385A>C
|
|
|
XR_924149.1:n.6264A>C
|
|
|
NM_001354579.1:c.6098A>C
|
NP_001341508.1:p.Tyr2033Ser
|
|
XR_001740179.2:n.6379A>C
|
|
|
XR_001740180.2:n.6433A>C
|
|
|
XR_001740181.2:n.6312A>C
|
|
|
XR_001740182.1:n.6264A>C
|
|
|
XR_002959543.1:n.6489A>C
|
|
|
XR_924148.2:n.6385A>C
|
|
|
NM_001184.4:c.6290A>C
MANE Select
|
NP_001175.2:p.Tyr2097Ser
|
|
NM_001354579.2:c.6098A>C
|
NP_001341508.1:p.Tyr2033Ser
|
|