ENST00000350026.11:c.3523G>T
|
ENSP00000055163.8:p.Val1175Phe
|
|
ENST00000414678.8:c.3592G>T
|
ENSP00000412835.3:p.Val1198Phe
|
|
ENST00000637015.2:c.3811G>T
|
ENSP00000489729.2:p.Val1271Phe
|
|
ENST00000319584.11:c.1696G>T
|
ENSP00000313006.7:p.Val566Phe
|
|
ENST00000346085.10:c.3562G>T
|
ENSP00000344546.5:p.Val1188Phe
|
|
ENST00000350026.10:c.3274G>T
|
ENSP00000055163.7:p.Val1092Phe
|
|
ENST00000414678.7:c.1840G>T
|
ENSP00000412835.2:p.Val614Phe
|
|
ENST00000635849.1:c.1003G>T
|
ENSP00000490948.1:p.Val335Phe
|
|
ENST00000635957.1:c.637G>T
|
ENSP00000490385.1:p.Val213Phe
|
|
ENST00000636930.2:c.3682G>T
MANE Select
|
ENSP00000490491.2:p.Val1228Phe
|
|
ENST00000636940.1:n.1679G>T
|
|
|
ENST00000637015.1:c.1050G>T
|
|
|
ENST00000637568.1:c.964G>T
|
|
|
ENST00000637741.1:n.348G>T
|
|
|
ENST00000637810.1:c.1024G>T
|
ENSP00000489636.1:p.Val342Phe
|
|
ENST00000637904.1:c.1183G>T
|
ENSP00000490550.1:p.Val395Phe
|
|
ENST00000647938.1:c.3313G>T
|
ENSP00000498155.1:p.Val1105Phe
|
|
ENST00000319584.10:c.1699G>T
|
ENSP00000313006.6:p.Val567Phe
|
|
ENST00000346085.9:c.3313G>T
|
ENSP00000344546.4:p.Val1105Phe
|
|
ENST00000350026.9:c.3274G>T
|
ENSP00000055163.7:p.Val1092Phe
|
|
ENST00000400790.3:c.475G>T
|
ENSP00000383596.3:p.Val159Phe
|
|
ENST00000414678.6:c.1840G>T
|
ENSP00000412835.2:p.Val614Phe
|
|
ENST00000478761.3:c.884G>T
|
|
|
NM_017519.2:c.3274G>T
|
NP_059989.2:p.Val1092Phe
|
|
NM_020732.3:c.3313G>T
|
NP_065783.3:p.Val1105Phe
|
|
XM_005267069.3:c.3433G>T
|
XP_005267126.2:p.Val1145Phe
|
|
XM_011535984.1:c.2512G>T
|
XP_011534286.1:p.Val838Phe
|
|
XM_011535985.1:c.2332G>T
|
XP_011534287.1:p.Val778Phe
|
|
XM_011535986.1:c.2092G>T
|
XP_011534288.1:p.Val698Phe
|
|
XM_011535987.1:c.1711G>T
|
XP_011534289.1:p.Val571Phe
|
|
XM_011535988.1:c.574G>T
|
XP_011534290.1:p.Val192Phe
|
|
NM_001346813.1:c.3433G>T
|
NP_001333742.1:p.Val1145Phe
|
|
NM_001363725.1:c.1183G>T
|
NP_001350654.1:p.Val395Phe
|
|
XM_011535984.2:c.3643G>T
|
XP_011534286.2:p.Val1215Phe
|
|
XM_011535988.3:c.574G>T
|
XP_011534290.1:p.Val192Phe
|
|
XM_017011103.2:c.3544G>T
|
XP_016866592.1:p.Val1182Phe
|
|
XM_017011104.1:c.3514G>T
|
XP_016866593.1:p.Val1172Phe
|
|
XM_017011105.2:c.3484G>T
|
XP_016866594.1:p.Val1162Phe
|
|
XM_017011106.2:c.3355G>T
|
XP_016866595.1:p.Val1119Phe
|
|
XM_017011107.2:c.3334G>T
|
XP_016866596.1:p.Val1112Phe
|
|
XR_002956289.1:n.3726G>T
|
|
|
NM_001363725.2:c.1183G>T
|
NP_001350654.1:p.Val395Phe
|
|
NM_001371656.1:c.3562G>T
|
NP_001358585.1:p.Val1188Phe
|
|
NM_001374820.1:c.3562G>T
|
NP_001361749.1:p.Val1188Phe
|
|
NM_001374828.1:c.3682G>T
MANE Select
|
NP_001361757.1:p.Val1228Phe
|
|
NM_017519.3:c.3523G>T
|
NP_059989.3:p.Val1175Phe
|
|