ENST00000350721.9:c.6298A>T
MANE Select
|
ENSP00000343741.4:p.Lys2100Ter
|
|
ENST00000513291.2:n.1482A>T
|
|
|
ENST00000654170.1:n.1141A>T
|
|
|
ENST00000656590.1:c.5088A>T
|
|
|
ENST00000661310.1:c.6106A>T
|
ENSP00000499589.1:p.Lys2036Ter
|
|
ENST00000665483.1:n.153A>T
|
|
|
ENST00000666447.1:n.133A>T
|
|
|
ENST00000666943.1:n.1762A>T
|
|
|
ENST00000350721.8:c.6298A>T
|
ENSP00000343741.4:p.Lys2100Ter
|
|
NM_001184.3:c.6298A>T
|
NP_001175.2:p.Lys2100Ter
|
|
XM_011512924.1:c.6304A>T
|
XP_011511226.1:p.Lys2102Ter
|
|
XM_011512925.1:c.6112A>T
|
XP_011511227.1:p.Lys2038Ter
|
|
XR_924147.1:n.6393A>T
|
|
|
XR_924148.1:n.6393A>T
|
|
|
XR_924149.1:n.6272A>T
|
|
|
NM_001354579.1:c.6106A>T
|
NP_001341508.1:p.Lys2036Ter
|
|
XR_001740179.2:n.6387A>T
|
|
|
XR_001740180.2:n.6441A>T
|
|
|
XR_001740181.2:n.6320A>T
|
|
|
XR_001740182.1:n.6272A>T
|
|
|
XR_002959543.1:n.6497A>T
|
|
|
XR_924148.2:n.6393A>T
|
|
|
NM_001184.4:c.6298A>T
MANE Select
|
NP_001175.2:p.Lys2100Ter
|
|
NM_001354579.2:c.6106A>T
|
NP_001341508.1:p.Lys2036Ter
|
|