ENST00000525626.6:n.662G>T
|
|
|
ENST00000528864.6:n.663G>T
|
|
|
ENST00000530813.2:c.*400G>T
|
ENSP00000508507.1:n.*400G>T
|
|
ENST00000682936.1:n.537G>T
|
|
|
ENST00000683307.1:c.51G>T
|
ENSP00000507198.1:p.Ala17=
|
|
ENST00000684249.1:n.965G>T
|
|
|
ENST00000685854.1:c.573G>T
|
ENSP00000508801.1:p.Ala191=
|
|
ENST00000686001.1:c.573G>T
|
ENSP00000508459.1:p.Ala191=
|
|
ENST00000687329.1:c.573G>T
|
ENSP00000510598.1:p.Ala191=
|
|
ENST00000689835.1:c.573G>T
|
ENSP00000510621.1:p.Ala191=
|
|
ENST00000690068.1:c.573G>T
|
ENSP00000509089.1:p.Ala191=
|
|
ENST00000692634.1:c.573G>T
|
ENSP00000508859.1:p.Ala191=
|
|
ENST00000693164.1:n.771G>T
|
|
|
ENST00000382409.4:c.777G>T
MANE Select
|
ENSP00000371846.3:p.Ala259=
|
|
ENST00000382409.3:c.777G>T
|
ENSP00000371846.3:p.Ala259=
|
|
ENST00000527170.5:c.139G>T
|
|
|
NM_001293634.1:c.664+1026G>T
|
NP_001280563.1:n.664+1026G>T
|
|
NM_021008.3:c.777G>T
|
NP_066288.2:p.Ala259=
|
|
XM_011519842.1:c.777G>T
|
XP_011518144.1:p.Ala259=
|
|
XM_011519843.1:c.777G>T
|
XP_011518145.1:p.Ala259=
|
|
XR_428838.2:n.783G>T
|
|
|
XR_930843.1:n.783G>T
|
|
|
XM_011519842.3:c.777G>T
|
XP_011518144.1:p.Ala259=
|
|
XM_024448325.1:c.777G>T
|
XP_024304093.1:p.Ala259=
|
|
XM_024448326.1:c.777G>T
|
XP_024304094.1:p.Ala259=
|
|
XM_024448327.1:c.777G>T
|
XP_024304095.1:p.Ala259=
|
|
NM_001367390.1:c.51G>T
|
NP_001354319.1:p.Ala17=
|
|
NM_021008.4:c.777G>T
MANE Select
|
NP_066288.2:p.Ala259=
|
|