ENST00000350721.9:c.6234T>C
MANE Select
|
ENSP00000343741.4:p.Tyr2078=
|
|
ENST00000513291.2:n.1418T>C
|
|
|
ENST00000654170.1:n.1077T>C
|
|
|
ENST00000656590.1:c.5024T>C
|
|
|
ENST00000661310.1:c.6042T>C
|
ENSP00000499589.1:p.Tyr2014=
|
|
ENST00000665483.1:n.89T>C
|
|
|
ENST00000666447.1:n.69T>C
|
|
|
ENST00000666943.1:n.1698T>C
|
|
|
ENST00000350721.8:c.6234T>C
|
ENSP00000343741.4:p.Tyr2078=
|
|
NM_001184.3:c.6234T>C
|
NP_001175.2:p.Tyr2078=
|
|
XM_011512924.1:c.6240T>C
|
XP_011511226.1:p.Tyr2080=
|
|
XM_011512925.1:c.6048T>C
|
XP_011511227.1:p.Tyr2016=
|
|
XR_924147.1:n.6329T>C
|
|
|
XR_924148.1:n.6329T>C
|
|
|
XR_924149.1:n.6208T>C
|
|
|
NM_001354579.1:c.6042T>C
|
NP_001341508.1:p.Tyr2014=
|
|
XR_001740179.2:n.6323T>C
|
|
|
XR_001740180.2:n.6377T>C
|
|
|
XR_001740181.2:n.6256T>C
|
|
|
XR_001740182.1:n.6208T>C
|
|
|
XR_002959543.1:n.6433T>C
|
|
|
XR_924148.2:n.6329T>C
|
|
|
NM_001184.4:c.6234T>C
MANE Select
|
NP_001175.2:p.Tyr2078=
|
|
NM_001354579.2:c.6042T>C
|
NP_001341508.1:p.Tyr2014=
|
|