ENST00000699485.1:c.520G>T
|
ENSP00000514396.1:p.Val174Phe
|
|
ENST00000362057.4:c.2176G>T
MANE Select
|
ENSP00000354623.3:p.Val726Phe
|
|
ENST00000674036.8:c.1149G>T
|
|
|
ENST00000674048.1:n.2057G>T
|
|
|
ENST00000265134.10:c.1027G>T
|
ENSP00000265134.6:p.Val343Phe
|
|
ENST00000362057.3:c.2176G>T
|
ENSP00000354623.3:p.Val726Phe
|
|
ENST00000374059.7:c.1123G>T
|
ENSP00000363172.3:p.Val375Phe
|
|
NM_001083885.2:c.1027G>T
|
NP_001077354.2:p.Val343Phe
|
|
NM_001173425.1:c.2176G>T
|
NP_001166896.1:p.Val726Phe
|
|
NM_015404.3:c.2176G>T
|
NP_056219.3:p.Val726Phe
|
|
XM_005251897.3:c.1513G>T
|
XP_005251954.2:p.Val505Phe
|
|
XM_011518484.1:c.2209G>T
|
XP_011516786.1:p.Val737Phe
|
|
XM_011518485.1:c.2209G>T
|
XP_011516787.1:p.Val737Phe
|
|
XM_011518486.1:c.2209G>T
|
XP_011516788.1:p.Val737Phe
|
|
XM_011518487.1:c.2083G>T
|
XP_011516789.1:p.Val695Phe
|
|
XM_011518488.1:c.1966G>T
|
XP_011516790.1:p.Val656Phe
|
|
XM_011518495.1:c.886G>T
|
XP_011516797.1:p.Val296Phe
|
|
XR_929747.1:n.3113G>T
|
|
|
XR_929748.1:n.3011G>T
|
|
|
NM_001346890.1:c.1123G>T
|
NP_001333819.1:p.Val375Phe
|
|
XM_011518486.2:c.2209G>T
|
XP_011516788.1:p.Val737Phe
|
|
XM_011518487.2:c.2083G>T
|
XP_011516789.1:p.Val695Phe
|
|
XM_011518488.2:c.1966G>T
|
XP_011516790.1:p.Val656Phe
|
|
XR_929747.2:n.2424G>T
|
|
|
XR_929748.2:n.2322G>T
|
|
|
NM_015404.4:c.2176G>T
MANE Select
|
NP_056219.3:p.Val726Phe
|
|
NM_001173425.2:c.2176G>T
|
NP_001166896.1:p.Val726Phe
|
|
NM_001083885.3:c.1027G>T
|
NP_001077354.2:p.Val343Phe
|
|