ENST00000350721.9:c.6264A>T
MANE Select
|
ENSP00000343741.4:p.Pro2088=
|
|
ENST00000513291.2:n.1448A>T
|
|
|
ENST00000654170.1:n.1107A>T
|
|
|
ENST00000656590.1:c.5054A>T
|
|
|
ENST00000661310.1:c.6072A>T
|
ENSP00000499589.1:p.Pro2024=
|
|
ENST00000665483.1:n.119A>T
|
|
|
ENST00000666447.1:n.99A>T
|
|
|
ENST00000666943.1:n.1728A>T
|
|
|
ENST00000350721.8:c.6264A>T
|
ENSP00000343741.4:p.Pro2088=
|
|
NM_001184.3:c.6264A>T
|
NP_001175.2:p.Pro2088=
|
|
XM_011512924.1:c.6270A>T
|
XP_011511226.1:p.Pro2090=
|
|
XM_011512925.1:c.6078A>T
|
XP_011511227.1:p.Pro2026=
|
|
XR_924147.1:n.6359A>T
|
|
|
XR_924148.1:n.6359A>T
|
|
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XR_924149.1:n.6238A>T
|
|
|
NM_001354579.1:c.6072A>T
|
NP_001341508.1:p.Pro2024=
|
|
XR_001740179.2:n.6353A>T
|
|
|
XR_001740180.2:n.6407A>T
|
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XR_001740181.2:n.6286A>T
|
|
|
XR_001740182.1:n.6238A>T
|
|
|
XR_002959543.1:n.6463A>T
|
|
|
XR_924148.2:n.6359A>T
|
|
|
NM_001184.4:c.6264A>T
MANE Select
|
NP_001175.2:p.Pro2088=
|
|
NM_001354579.2:c.6072A>T
|
NP_001341508.1:p.Pro2024=
|
|