ENST00000236671.7:c.986G>T
MANE Select
|
ENSP00000236671.2:p.Cys329Phe
|
|
ENST00000367196.4:c.881G>T
|
ENSP00000356164.4:p.Cys294Phe
|
|
ENST00000427721.3:c.411G>T
|
|
|
ENST00000429746.2:c.881G>T
|
ENSP00000402586.2:p.Cys294Phe
|
|
ENST00000433655.6:c.*152G>T
|
ENSP00000404902.1:n.*152G>T
|
|
ENST00000438213.6:c.1103G>T
|
ENSP00000415036.2:p.Cys368Phe
|
|
ENST00000497544.3:n.694G>T
|
|
|
ENST00000636397.1:c.986G>T
|
ENSP00000489910.1:p.Cys329Phe
|
|
ENST00000636571.1:c.965G>T
|
ENSP00000490770.1:p.Cys322Phe
|
|
ENST00000636615.1:c.986G>T
|
ENSP00000490014.1:p.Cys329Phe
|
|
ENST00000636843.1:c.980G>T
|
ENSP00000490897.1:p.Cys327Phe
|
|
ENST00000637158.1:n.584G>T
|
|
|
ENST00000637381.2:n.3414G>T
|
|
|
ENST00000637387.1:c.973-8G>T
|
ENSP00000490598.1:n.973-8G>T
|
|
ENST00000637815.2:c.968G>T
|
ENSP00000490344.1:p.Cys323Phe
|
|
ENST00000637915.1:c.986G>T
|
ENSP00000490471.1:p.Cys329Phe
|
|
ENST00000637937.1:n.294G>T
|
|
|
ENST00000678991.1:c.*847G>T
|
ENSP00000503019.1:n.*847G>T
|
|
ENST00000236671.6:c.986G>T
|
ENSP00000236671.2:p.Cys329Phe
|
|
ENST00000427721.2:c.386G>T
|
ENSP00000415840.2:p.Cys129Phe
|
|
ENST00000429746.1:c.317G>T
|
ENSP00000402586.1:p.Cys106Phe
|
|
ENST00000433655.5:c.*152G>T
|
ENSP00000404902.1:n.*152G>T
|
|
ENST00000497544.1:n.694G>T
|
|
|
NM_001909.4:c.986G>T
|
NP_001900.1:p.Cys329Phe
|
|
NM_001909.5:c.986G>T
MANE Select
|
NP_001900.1:p.Cys329Phe
|
|