ENST00000526008.6:c.*856A>T
|
ENSP00000513006.1:n.*856A>T
|
|
ENST00000696967.1:n.1476A>T
|
|
|
ENST00000696970.1:n.954A>T
|
|
|
ENST00000458235.7:c.2299A>T
MANE Select
|
ENSP00000391676.1:p.Arg767Trp
|
|
ENST00000458235.5:c.2299A>T
|
ENSP00000391676.1:p.Arg767Trp
|
|
ENST00000527031.5:n.2278+2105A>T
|
|
|
ENST00000527670.5:c.2299A>T
|
ENSP00000432511.1:p.Arg767Trp
|
|
ENST00000534444.1:c.2299A>T
|
ENSP00000436421.1:p.Arg767Trp
|
|
NM_000215.3:c.2299A>T , LRG_77t1:c.2299A>T
|
NP_000206.2:p.Arg767Trp
|
|
XM_005259896.2:c.2428A>T
|
XP_005259953.1:p.Arg810Trp
|
|
XM_006722745.2:c.2299A>T
|
XP_006722808.1:p.Arg767Trp
|
|
XM_011527990.1:c.2428A>T
|
XP_011526292.1:p.Arg810Trp
|
|
XR_430137.2:n.2438A>T
|
|
|
XM_005259896.3:c.2428A>T
|
XP_005259953.1:p.Arg810Trp
|
|
NM_000215.4:c.2299A>T
MANE Select
|
NP_000206.2:p.Arg767Trp
|
|