ENST00000350721.9:c.6531G>A
MANE Select
|
ENSP00000343741.4:p.Trp2177Ter
|
|
ENST00000513291.2:n.1715G>A
|
|
|
ENST00000654170.1:n.1374G>A
|
|
|
ENST00000656590.1:c.5321G>A
|
|
|
ENST00000661310.1:c.6339G>A
|
ENSP00000499589.1:p.Trp2113Ter
|
|
ENST00000665483.1:n.386G>A
|
|
|
ENST00000666447.1:n.366G>A
|
|
|
ENST00000666943.1:n.1995G>A
|
|
|
ENST00000350721.8:c.6531G>A
|
ENSP00000343741.4:p.Trp2177Ter
|
|
ENST00000513291.1:c.70G>A
|
|
|
NM_001184.3:c.6531G>A
|
NP_001175.2:p.Trp2177Ter
|
|
XM_011512924.1:c.6537G>A
|
XP_011511226.1:p.Trp2179Ter
|
|
XM_011512925.1:c.6345G>A
|
XP_011511227.1:p.Trp2115Ter
|
|
XR_924147.1:n.6626G>A
|
|
|
XR_924148.1:n.6626G>A
|
|
|
XR_924149.1:n.6505G>A
|
|
|
NM_001354579.1:c.6339G>A
|
NP_001341508.1:p.Trp2113Ter
|
|
XR_001740179.2:n.6620G>A
|
|
|
XR_924148.2:n.6626G>A
|
|
|
NM_001184.4:c.6531G>A
MANE Select
|
NP_001175.2:p.Trp2177Ter
|
|
NM_001354579.2:c.6339G>A
|
NP_001341508.1:p.Trp2113Ter
|
|